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FOOD AND DRUG ADMINISTRATION COMPLIANCE PROGRAM GUIDANCE MANUAL PROGRAM 7348.808A
View & download of more than 71 Midtronics PDF user manuals, service manuals, operating guides. Measuring Instruments, user manuals, operating guides & specifications. Battery charger NAPA model 85-302 -manual. Napa Essentials Battery Charger 85-302. Battery charger from Napa 85327. Napa Essentials Battery Charger 85327. Need schematic. Napa Essentials Battery Charger 85-1010. MDX-P300 Battery & Electrical System Analyzer. Complete with an integrated printer, the Midtronics MDX-P300 makes it easy and affordable to determine and present the current state of a battery and electrical system. This manual is detailed with hundreds of photos, pictures and illustrations to help guide you through repair procedures. It will help you understand, care for, and lower the repair and maintenance cost for your Suzuki Outboard Engine (motor) for a overall improved satisfaction with your ownership. Midtronics products are designed to meet a variety of battery and electrical system service requirements, but selected features on individual products may make them a better fit for your unique service applications. This product is particularly well-suited for these battery management processes.
Date of Issuance: 94-24 08/25/00 FORM FDA 2438 PAGE 1
Subject
GOOD LABORATORY PRACTICE PROGRAM
(Nonclinical Laboratories)
EPA DATA AUDIT INSPECTIONS
GOOD LABORATORY PRACTICE PROGRAM
(Nonclinical Laboratories)
EPA DATA AUDIT INSPECTIONS
Implementation Date
October 1, 2000
October 1, 2000
Completion Date
September 30, 2003
September 30, 2003
Data Reporting
Product Codes | Product/Assignment Codes | ||
---|---|---|---|
52Y | 04808A - Chemical Contaminants |
Field Reporting Requirements
Inspections covered by this compliance program involve facility inspections and data audits conducted under Food and Drug Administration (FDA) authority and data audits conducted under authority delegated to FDA by the Environmental Protection Agency (EPA). Separate establishment inspection reports (EIR) should be prepared for the FDA and EPA components of the inspection. For the FDA component of the inspection, the EIR including attachments and exhibits, will be sent to the assigning center bioresearch monitoring program unit. For the EPA component, the EIR including attachments and exhibits, and inspectional support documents provided by EPA prior to the inspection, will be sent to the Office of Enforcement, Division of Compliance Policy (HFC-230). The District Office should NOT retain any records or documents related to EPA component of the inspection.
For data reporting purposes, all manpower expenditures on EPA assignments by FDA investigators; such as pre-inspection activities, on-site time, and report writing, should be fully reported as EPA time expenditures under 7348.808A on the same cover sheet as the FDA component of the inspection under 7348.808.
PART I - BACKGROUND
An Interagency Agreement between the Food and Drug Administration (FDA) and the Environmental Protection Agency (EPA) provides for FDA auditing of selected health-related toxicological test reports and related laboratory records in order for EPA to determine, (1) whether the testing was performed in accordance with the test protocols, (2) whether any reported deviations may have affected the reliability of the test results, and (3) whether the test reports fully and accurately reflected the test procedures and results. These audits will be performed by making on-site visits of the toxicological laboratories that conducted the tests. The agreement is limited to coverage of laboratories within the United States.
EPA is responsible for setting tolerances for pesticide residues in or on raw agricultural commodities and processed foods under the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 346 and 348) and for registering pesticides under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) (7 U.S.C. 136 etsec). In addition, EPA has the mandated task under the Toxic Substances Control Act (TSCA) (15 U.S.C. 2601) to assure that no chemical will present an unreasonable risk of injury to health or the environment. EPA regulatory decisions on such matters are based in part on the results of toxicological testing performed by or for registration applicants, tolerance petitioners, and chemical manufacturers. Therefore, it is essential that such testing provide an objective and reliable basis for decision-making. An EPA determination that testing was deficient or that a test report was inadequate, may lead to regulatory and/or enforcement action; accordingly, such determinations must be well founded and fully documented.
PART II - IMPLEMENTATION
Objective
This program is designed to provide specific instructions regarding the conduct of EPA data audit inspections under the Good Laboratory Practice Program (CP 7348.808).
Program Management Instructions
- Kinds of Laboratories to be Inspected
- See CP 7348.808
- FDA may perform data audit inspections for EPA at facilities which test pesticides or toxic substances not regulated by FDA.
- Frequency and Type of Inspection
- The laboratories identified by EPA for coverage under this program will be inspected in accordance with assignments issued to FDA district offices by HFC-230.
- Each inspection may include a detailed audit of one or more studies to determine whether: (1) the final laboratory report(s) submitted to EPA, accurately reflects the raw data, (2) the testing was performed in a manner that did not involve errors or practices that may have adversely affected the validity of the study, and (3) the testing was performed in accordance with the protocol submitted to EPA.
- Inspection Team EPA may provide a staff scientist or regional inspector to accompany the FDA investigator. EPA may waive this whenever scientific support is not deemed necessary for carrying out the objectives of an audit.
- Team Leader: The FDA investigator, as team leader, has the prime responsibility for the accomplishment and theconduct of joint inspections involving EPA agency personnel. Additional FDA field investigators may participate at the discretion of the district.
- EPA Participant: EPA personnel will serve in a scientific advisory capacity to the team leader and shall specifically participate in the inspection by:
- attending any scheduled pre-inspection conferences, and
- participating in the on-site inspection and remaining on-site with the FDA investigator for as long as necessary to complete the audit of studies being examined.
- Should the EPA scientist depart and, in the judgment of the FDA investigator, the data audit inspection cannot be continued without the aid of the scientist, the district will immediately inform the HFC-230 contact. If the inspection is terminated, the district will prepare an inspection report encompassing only those studies audited prior to termination.
- Disagreements between FDA investigators and EPA staff regarding conduct of inspection should be discussed off-site and if not resolved, should be immediately referred to the HFC-230 contact.
Written signed observations of the EPA participants regarding this data audit inspection must be included in the report submitted to EPA. It is important that the EPA participant provide the FDA investigator with all comments or observations on the inspection before his/her departure from the district. - Confirmation of Schedule After the district has scheduled a tentative inspection date, the district will advise the EPA contact of the anticipated date of inspection.If EPA is to participate in the data audit inspection, the district will inform the EPA contact as soon as possible to permit the coordination of schedules. Joint inspection arrangements should be agreeable to both parties, with no undue delays by either party.
- Prior Notification of the Facility to be Inspected EPA may notify the sponsor of the study to be audited in order to request that the sponsor provide test substance characterization data to the nonclinical laboratory.FDA prior notification of the laboratory facility will be done in accordance with CP 7348.808.
PART III - INSPECTIONAL
Establishment Inspections
- Authority to Audit EPA Studies FDA investigators will be delegated the authority to review records under Sections 8 and 22 of FIFRA and/or Sections 9 and 11 of TSCA. The delegation of authority will be documented in a ALetter of Entry@ provided to the investigator(s) by the EPA contact.
- Inspectional Procedures for EPA Data Audits After displaying FDA credentials and issuing a Form FDA-482, the lead investigator should inform testing facility management of the reason for and the intended scope of the inspection. This will include information that the inspection will include the physical facility, if applicable, a data audit of FDA selected studies, and under the authority of the EPA Letter of Entry, will also include a data audit of EPA selected studies. The EPA Letter of Entry will include a statement that confidential commercial or trade secret, or other non-public information that the facility provides to FDA during the data audit of EPA studies will be given by FDA to EPA. The lead investigator should also advise the testing facility management that any study records copied from an EPA study and any written report of any observations made during the EPA data audit portion of the inspection including confidential commercial, trade secret, or other non-public information, will be submitted directly to EPA for appropriate review and follow-up by that agency. It is suggested that the EPA data audit portion of the inspection should be conducted after the inspectional operations for FDA regulated studies and facilities under CP 7348.808 are completed. The data audit procedures found in CP 7348.808, Part III-Inspectional, D. Data Audit, may be useful guidance for conducting the EPA requested data audit portion of the inspection under CP 7348.808A.
- Issuance of an FDA-483
- Inspectional observations under FDA authority An FDA-483 will be issued under this program when noncompliance with FDA GLP regulations is observed and the laboratory is or has worked on FDA-regulated products
- Data audit observations under EPA delegated authority
Inspectional observations during the EPA data audit portion of the inspection should be recorded separately from observations related to noncompliance with FDA GLP regulations. The observations may be listed on a Form FDA-483 provided that the references to FDA laws on the back of the Form FDA-483 are omitted or crossed through. It should be noted on the Form FDA-483 that the observations are being provided under authority delegated from EPA to FDA in the EPA Letter of Entry. - Refusal to Permit Inspection Refusal to permit inspection or copying of records should be reported immediately to HFC-230, telephone 301-827-0420.
- Confidentiality Under various provisions of the FD&C Act, FIFRA, and TSCA, data submitted in support of tolerance petitions and registration applications may be considered trade secrets or confidential business information entitled to protection from unauthorized public disclosure.FDA will maintain the confidentiality of all data received as a result of an inspection conducted for EPA. The FDA district office will NOT retain a copy of the EPA audit report. Any requests for disclosure of such information received by the FDA under the Freedom of Information Act or other non-EPA requester will be referred to EPA for processing and response. All documents provided to FDA by EPA for the conduct of the audits will be returned to EPA along with the audit report.
- Report Format Follow the report format outlined in CP 7348.808.
PART IV - ANALYTICAL
No samples are to be collected under this program circular.
PART V - REGULATORY / ADMINISTRATIVE STRATEGY
FDA Inspection
See CP 7348.808
EPA Data Audit
EPA will determine whether discrepancies listed in reports submitted by FDA investigators impact on the validity of the audited studies. Any administrative or regulatory actions resulting from EPA audit reports will be the responsibility of EPA and will be consistent with TSCA or FIFRA regulations.
Exchange of Information
Each agency will exchange information and coordinate actions concerning active investigations, regulatory correspondence and legal or administrative action being considered against any laboratory covered under this agreement. In addition to the provisions of III. E., FDA will disclose information from its records to EPA according to FDA's procedures to implement 21 CFR 20.85.
PART VI - REFERENCES AND CONTACTS
References
- 40 CFR Part 792, Toxic Substances Control; Good Laboratory Practices Standards.
- 40 CFR Part 160, Pesticide Programs, Good Laboratory Practice Standards.
- 21 CFR Part 58, Good Laboratory Practice for Nonclinical Laboratory Studies.
- 21 CFR 20.85, Disclosure to other Federal government departments and agencies.
- Compliance Program Guidance Manual 7348.808; Chapter 48 - Bioresearch Monitoring, Good Laboratory Practice.
Program Contacts
When technical questions arise on a specific assignment, or when additional information or guidance is required, contact the assigning Center. Operational questions should be addressed to HFC-130.
Specific Contacts
Office of the Associate Commissioner for Regulatory Affairs
Office of Enforcement, Division of Compliance Policy: Robert Hummel, DBA, HFC-230, 240-632-6845, FAX 240-632-6861.
Office of Regional Operations, Division of Field Investigations: Ruark Lanham, HFC-130, 301-827-6691, FAX 301-443-3757.
Office of Compliance, Laboratory Data Integrity Branch (2225A), Ariel Rios Building, 1200 Pennsylvania Avenue, N.W., Washington, D.C. 20460 (when sending documents via an express service use the ZIP code 20004 and list the room number as 5109), Ms. Francisca Liem, 202-564-2365, FAX 202-564-0029.
Center for Drug Evaluation and Research (CDER)
Office of Compliance, Division of Scientific Investigations: Joseph Salewski, HFD-45, 301-796-3395, FAX 301-847-8748.
Center for Biologics Evaluation and Research (CBER)
Bioresearch Monitoring Staff: Patricia Holobaugh, HFM-664, 301-827-6347, FAX 301-827-6748.
Center for Veterinary Medicine (CVM)
Bioresearch Monitoring Staff: Mr. Vernon Toelle, Ph.D., HFV-234, 240-276-9238, FAX 240-276-9241.
Center for Devices and Radiological Health (CDRH)
Division of Bioresearch Monitoring: Michael Marcarelli, HFZ-311, 301-796-5629, FAX 301-847-8136.
Center for Food Safety and Applied Nutrition (CFSAN)
Office of Food Additive Safety, Division of Petition Review: Catherine Whiteside, Ph.D., HFS-265, 301-436-1265, FAX 301-436-2972.
PART VII – HEADQUARTER’S RESPONSIBILITIES
Office of Regulatory Affairs
Office of Enforcement, Division of Compliance Policy (HFC-230)
- Is the liaison with EPA concerning the nonclinical laboratory compliance program.
- Conducts periodic meetings with EPA and FDA centers to identify facilities requiring a coordinated inspection under the interagency agreement.
- Following consultation with EPA, issue assignments to the district offices with copies to HFC-130 and the appropriate center for inspections coordinated under the interagency agreement.
- Receives and reviews EIRs of EPA data audits and approves the forwarding of the documents to the EPA contact.
- Reviews and resolves pertinent differences in the classification of the EPA data audit and the FDA inspection.
- Notifies EPA whenever FDA approves a regulatory action against a specific laboratory.
- Advises district offices in managing refusals to permit inspection.
Office of Regional Operations, Division of Emergency and Investigational Operations (HFC-130)
- Monitors inspectional operations.
Centers
- Attend periodic meetings with EPA to identify facilities requiring coordinated inspection under the interagency agreement.
- Communicate final inspection classification of the FDA inspection to HFC-230 and the EPA contact.
EPA Contact Responsibilities
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- Is the liaison with FDA concerning the nonclinical laboratory compliance program.
- Attends periodic meetings with FDA representatives to identify facilities requiring a coordinated inspection under the interagency agreement.
- Following consultation with FDA, provides FDA liaison with pre-inspectional documents to be used in conducting EPA data audits.
- Provides investigators with a letter of entry delegating authority to FDA to audit test data submitted to EPA.
- Communicates final inspection classification of the EPA data audit to FDA liaison.
- Reviews and resolves pertinent differences in the classification of the EPA data audit and the FDA inspection.
- Notifies FDA whenever EPA approves a regulatory action against a laboratory.
- Provides information for updating the FDA's list of GLP Inspections.
.
Service Manual Application: Suzuki Workshop Service Manual DT 2 THRU 225 HP 1988, 1989, 1990, 1991, 1992, 1993, 1994, 1995, 1996, 1997, 1998, 1999, 2000, 2001, 2002, 2003 DT Outboard Engines.
This workshop service repair manual gives step by step information on maintenance, repair and mechanic overhaul. This manual is detailed with hundreds of photos, pictures and illustrations to help guide you through repair procedures. It will help you understand, care for, and lower the repair and maintenance cost for your Suzuki Outboard Engine (motor) for a overall improved satisfaction with your ownership.
MODELS & YEARS COVERED:
DT2 (DT-2) 1988, 1989, 1990, 1991, 1992, 1993, 1994, 1995 & 1996
DT2.2 (DT-2.2) 1997
DT4 (DT-4) 1988, 1989, 1990, 1991, 1992, 1993, 1994, 1995, 1996, 1997 & 1998
DT5Y (DT-5-Y) 1998, 1999, 1991, 1992, 1993, 1994, 1995, 1996, 1997, 1999, 2000, 2001 & 2002
DT6 ( DT-6) 1988, 1989, 1990, 1991, 1992, 1993, 1994, 1995, 1996 & 1997
DT8 (DT-8) 1988, 1989, 1990, 1991, 1992, 1993, 1994, 1995, 1996 & 1997
DT9.9 ( DT-9.9) 1988 thru 1997
DT15 (DT-15) 1988-1989
DT20 (DT-20) 1988
DT25 (DT-25) 1990-1991
DT30 (DT-30) 1989-1997
DT35 (DT-35) 1988-1997
DT40 (DT-40) 1988-1998
DT55 (DT-55) 1988-1997
DT65 (DT-65) 1988-1997
DT75 (DT-75) 1988-1997
DT85 (DT-85) 1988-2000
DT90 (DT-90) 1989-1997
DT100 (DT-100) 1989-1996 & 1996-2001 EFI
DT140 (DT-140) 1988-1996 & 1996-2001 EFI
DT150 (150) 1988-1994 & 1995, 1996, 1997, 1998, 1999, 2000, 2001, 2002 & 2003 EFI
DT2.2 (DT-2.2) 1997
DT4 (DT-4) 1988, 1989, 1990, 1991, 1992, 1993, 1994, 1995, 1996, 1997 & 1998
DT5Y (DT-5-Y) 1998, 1999, 1991, 1992, 1993, 1994, 1995, 1996, 1997, 1999, 2000, 2001 & 2002
DT6 ( DT-6) 1988, 1989, 1990, 1991, 1992, 1993, 1994, 1995, 1996 & 1997
DT8 (DT-8) 1988, 1989, 1990, 1991, 1992, 1993, 1994, 1995, 1996 & 1997
DT9.9 ( DT-9.9) 1988 thru 1997
DT15 (DT-15) 1988-1989
DT20 (DT-20) 1988
DT25 (DT-25) 1990-1991
DT30 (DT-30) 1989-1997
DT35 (DT-35) 1988-1997
DT40 (DT-40) 1988-1998
DT55 (DT-55) 1988-1997
DT65 (DT-65) 1988-1997
DT75 (DT-75) 1988-1997
DT85 (DT-85) 1988-2000
DT90 (DT-90) 1989-1997
DT100 (DT-100) 1989-1996 & 1996-2001 EFI
DT140 (DT-140) 1988-1996 & 1996-2001 EFI
DT150 (150) 1988-1994 & 1995, 1996, 1997, 1998, 1999, 2000, 2001, 2002 & 2003 EFI
DT175 (175) 1988-1992
DT200 (200) 1988-1992 & 1993-2000 EFI
DT225 (225) 1990-2003
DT200 (200) 1988-1992 & 1993-2000 EFI
DT225 (225) 1990-2003
SUPPLEMENT MANUAL- ADDITIONAL SERVICE DATA FOR 1999 & LATER MODELS (1999+ MODELS) INCLUDING CARBURETOR & IGNITION COIL SPECIFICATIONS.
1999+ DT4/DT5Y
1999+ DT5 DT6 & DT8
1999+ DT25C DT30C (DT25-C, DT30-C)
1999+ DT75 & DT85
1999+ DT100TC
1999+ DT115STC & DT140TC EFI (DT115-STC, DT140-TC)
1999+ DT150 / 175 / 200
1999+ DT225 M
1999+ DT5 DT6 & DT8
1999+ DT25C DT30C (DT25-C, DT30-C)
1999+ DT75 & DT85
1999+ DT100TC
1999+ DT115STC & DT140TC EFI (DT115-STC, DT140-TC)
1999+ DT150 / 175 / 200
1999+ DT225 M
Below is a SMALL sample of some of the chapters including some of the information contained in each chapter. There are many more chapters and data in this manual.
CHAPTERS
Midtronics A087 Printer Manual
GENERAL INFORMATION
How To Use This Manual: can you do it, where to begin, avoiding trouble, maintenance or repair, directions and locations, professional help, purchasing parts, avoiding the most common mistakes.
Boating Saftey: regulations for your boat, documenting of vessels, registration of boats, numbering of vessels, sales and transfers, hull identification number, length of boats, capacity information, certificate of compliance, ventilation & systems, required saftey equipment, sound producing devices and much more.
Saftey In Service: dos & donts.
TOOLS & EQUIPMENT
Tools And Equipment: safety tools, work gloves, eye/ear protection, work clothes, chemicals, lubricants & penetrates, sealants, cleaners.
Tools: hand tools, socket sets, wrenches, pliers, screwdrivers, hammers, other common tools, special tools, electronic tools, gauges, measuring tools, micrometers & Calipers, dial indicators, telescoping gauges, depth gauges.
Fasteners/Measurements & Conversions: bolts, nuts & other threaded retainers, torque, standard and metric measurements.
Specifications Charts: conversion factors
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MAINTENANCE
Engine Maintenance: serial number identification, 2-stroke oil, oil recommendations, filling, lower unit, draining & filling, fuel filter, relieving fuel system pressure, removal and installation, fuel/water separator, trim/tilt pivot points, inspection and lubrication, propeller.
Boat Maintenance: inside the boat, fiberglass hulls, trim tabs, adodes and lead wires, battery/cleaning/checking specific gravity/terminals/charging & safety/replacing battery cables.
Tune-UP: introduction, tune-up sequence, compression check, checking compression, low compression, spark plugs, spark plug heat range, spark plug service, removal and installation, spark plug gap, spark plug wires, timing and synchronization, DT2 (DT2.2) ignition timing, idle speed, DT4, DT6, DT9.9 and DT15, DT-15.
FUEL SYSTEM
Fuel and Combustion: fuel recommendations, octane rating, vapor pressure and additives, the bottom line with fuels, high altitude operation, alcohol blended fuels, abnormal combustion, factors affecting combustion.
Fuel System: carburetion, general information, carburetor circuits, basic functions, dual throat carburetors, removing fuel from the system, fuel pump.
Troubleshooting: fuel system, logical troubleshooting, common problems, fuel pump, fuel line, common broblems, combustion related piston failures.
Carburetor Service: DT2 & DT-2.2, removal, installation, disassembly, cleaning, inspection, assembly, DT4 & DT5Y, DT6 (DT-6) and 1988 DT8 (DT-8), DT20 (DT-20) to DT85, DT115 (DT-115), DT140 ( DT-140), V4 & V6 powerheads, DT4 THRU DT85, DT90 Thru DT200.
IGNITION & ELECTRICAL
Understanding and Troubleshooting Electrical Systems: basic electrical theory, how electricity works, water analogy, ohms, electrical components, power source, ground, protective devices, swithes & relays, load, wiring & harnesses, connectors, test equipment, jumper wired, test lights, open circuits, short circuits, wire and connector repair, electrical system precautions and much more.
Breaker Points Ignition (MAGNETO IGINITION): system testing, breaker points, point gap adjustment testing, condenser, ignition coil testing/removal/installation and much more.
Capacitor Discharge Ignition CDI System: description and operation, single cylinder ignition, Suzuki PEI ignition, System testing procedure, pulsar, charging gear counter coils, ignition coils, CDI unit and more.
Midtronics Inspect 85 Manual Download
OIL INJECTION
Oil Injection System: description and operation, oil pump, air/oil mixing valve, troubleshooting the oil injection system, bleeding the oil injection system, oil tank, oil pump, oil lines, oil pump discharge rate testing & adjustment, oil pump control rod adjustment.
Cooling System: water pump, thermostat, removal, installation, cleaning, inspection.
Midtronics Inspect 85 Manual Pdf
Oil Injection warning System: Low oil level, oil flow, troubleshooting the oil injection warning system, oil level sensor, oil flow sensor.
Overheat Warning System: overheat sensor, testing, removal, installation, light, buzzer.
POWER HEAD
Engine Mechanical: the two stroke cycle, flywheel removal, installation, inspection, powerhead, disassembly & assembly.
Powerhead Reconditioning: determine powerhead condition, primary compression test, secondary compression, buy or rebuild, powerheand overhaul tips, tools, cautions, cleaning, reaping damaged threads, power head preparation, cylinder block and head, general information, inspection, cylinder bores, pistons, piston pins, piston rings, connecting rods, the crankshaft, bearings.
Powerhead Reconditioning: determine powerhead condition, primary compression test, secondary compression, buy or rebuild, powerheand overhaul tips, tools, cautions, cleaning, reaping damaged threads, power head preparation, cylinder block and head, general information, inspection, cylinder bores, pistons, piston pins, piston rings, connecting rods, the crankshaft, bearings.
Specifications Charts: Torque Specs, engine rebuilding specs & specifications.
LOWER UNIT
Lower Unit: general information, shifting principles, standard rotating unit, counter roatating unit, troubleshooting the lower unit, propeller removal & installation, lower unit, no reverse gear, lower unit with reverse gear.
Lower Unit Overhaul includes disassembly, cleaning, inspection, assembly, shimming procedure: DT4, DT5Y, DT6, DT8, DT9.9, DT15, DT20, DT25, DT30, DT35, DT40, DT55, DT65, DT75, DT85, DT115, DT140, V4 & V6, JET Drive
TRIM & TILT
Manual tilt, gas assist tilt, power tilt, power trim tilt and more.
Suzuki Workshop Service Manual, Owners Workshop Manual, Repair Guide, Repair Manual, 2hp, 2.2hp, 4hp, 5hp, 6hp, 8hp, 9.9hp, 15hp, 20hp, 25hp, 30hp, 35hp, 40hp, 55hp, 65hp, 75hp, 85hp, DT-90hp, 100hp, 140hp, 150hp, 175hp, 200 hp, 225hp, 1988, 1989, 1990, 1991, 1992, 1993, 1994, 1995, 1996, 1997, 1998, 1999, 2000, 2001, 2002, 2003, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 00, 01, 02, 03