Definition of family of parts - PPAP Sec.II - FORD Specific Instructions

M

Micaelah Ash

#1
#1
Please tell me the definition of family of parts.(PPAP Sec.II FORD Specific Instructions)
Original product and revised product?
Old model and new model?

Any help is greatly appreciated.
Thanks in advance.
 
Standard Work Instruction Software by Dozuki
Elsmar Forum Sponsor
S

Sam

#2
#2
IMO, "family" means parts that share the same the same basic construction and processing.
I worked for a company that Mfg. air,oil, and fuel filters for the OEM market.
While there are 100's of different kinds of each filter, I only needed three FMEA's and three Control Plan's (one for each type) because each type of filter was processed under the same conditions.
 
S

Spaceman Spiff

#3
#3
A family of parts means that various part numbers have the same type configuration. For example, in my last job we made sensors for automotive application. The sensors look identical except the electrical resistance values. Hope that helps.
 
J

Jim Biz

#4
#4
We have "family of parts"
Steel SPACERS
Part number 1036) 25.0mm outside diameter 20.0mm inside - 15.0mm long
Part number 1037) 25.0mm outside diameter 20.0mm inside diameter 25.0mm long
Part number 1038) 25.0 mm outside diameter 20.0mm otside diameter 40.0 long

All 3 make up "family" (or) group of like parts.

Origional Part Revision A in change block on blueprint...
Revised part - revision B on blueprint
 
M

Micaelah Ash

#5
#5
Thank you very much for your help!
I understood definition of "family of parts".
BTW, Does anyone know some BIG3's official documents which describes definition of "family of parts" in a glossary or whatelse?
If you have it, please tell me what says it.

Thank you again.
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
L 'Distributor' definition & MDR/MSR relationship EU Medical Device Regulations 1
D Definition of equipment for ISO 13485:2016 ISO 13485:2016 - Medical Device Quality Management Systems 0
M ISO 13485:2016 Complaint Definition Clarity Customer Complaints 2
DuncanGibbons Technical Data Package vs Digital Product Definition APQP and PPAP 0
S Definition of "worldwide" in view of IATF 16949 and Product conformity IATF 16949 - Automotive Quality Systems Standard 3
S Importer definition EU Medical Device Regulations 0
A Software as Medical Device (SaMD) definition and its applicability Other Medical Device and Orthopedic Related Topics 4
M Definition of Done - New Product Phase to the sustaining phase Manufacturing and Related Processes 3
M Help me improve the definition for internal PPM Manufacturing and Related Processes 3
D Tolerance definition based on expected Cp/cpk Reliability Analysis - Predictions, Testing and Standards 14
D BS EN 62304 - Medical-Relevant Data C.5 - Definition of IEC 62304 - Medical Device Software Life Cycle Processes 5
P Definition of production tooling in IATF16949 clause 8.5.1.6 IATF 16949 - Automotive Quality Systems Standard 4
J Sample size definition in an Automotive SMT pilot lot run Misc. Quality Assurance and Business Systems Related Topics 1
J Here is my definition of Defect Mapping Quality Tools, Improvement and Analysis 2
D Definition of "Critical Laboratory Equipment"? General Measurement Device and Calibration Topics 1
Z Definitive definition of design? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
R Definition Key Supplier - Definition of Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 7
A Definition of customer in ITP (Inspection & Test Plan) Contract Review Process 3
F MEDDEV 2.7/1 rev 4 and MDR - Definition of Description of Principles of operation EU Medical Device Regulations 4
S Definition of "servicing activities" - Spinal Implants ISO 13485:2016 - Medical Device Quality Management Systems 4
T Custom made medical device MDD vs MDR definition CE Marking (Conformité Européene) / CB Scheme 12
C Function definition for DFMEA FMEA and Control Plans 1
W Key functional characteristic definition - Tolerances and Deviations Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 0
Marc Definition Waiver - Definition Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 4
M Informational MHRA guidance – Assistive technology: definition and safe use Medical Device and FDA Regulations and Standards News 0
R Critical suppliers (Definition of) and MDSAP (Medical Device Single Audit Program) ISO 13485:2016 - Medical Device Quality Management Systems 15
Pancho Definition Quality Assurance Program - Definition Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 9
M Inputs on definition of very similar processes for multi site audit sample - IAF MD1 2018 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
U Hand-Held dosing device has no PATIENT - Interpretation of the PATIENT definition IEC 60601 - Medical Electrical Equipment Safety Standards Series 6
L Medical Device Accessory - Health Canada guidance / definition on what an accessory is Canada Medical Device Regulations 3
C MDR Importer/Distributor Definition Questions EU Medical Device Regulations 5
G Medical Device "Immediate Container" Interpretation of Definition US Food and Drug Administration (FDA) 2
S Definition of Convenience Kit for a Combination Product US Food and Drug Administration (FDA) 0
M Are Risks and Opportunities Required as Part of the Process Definition ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
A Definition of "Sensitive Products" Clause 8.5.4 (c) in AS9100 Rev. D AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
Marc Definition Jidoka - Definition Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 2
Marc Definition DFMEA (Design FMEA) - Definition Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 0
J Definition of repackager v. manufacturer 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
S MDR Annex II Design & Manufacturing info - 'Adjuvants' definition EU Medical Device Regulations 3
C Informational CFR 21 Definition for Data or Raw Data Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 5
I Lot or Batch definition for IVDs Imported Legacy Blogs 0
S Mains outlet MSO definition IEC 60601 - Medical Electrical Equipment Safety Standards Series 0
Mikishots Definition Defined - Definition and meaning of "defined" Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 10
D Definition User Needs - Concrete definition for "User Needs" as required by the FDA Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 2
L Process Definition and Process Validation 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
B MDD or MDR Definition of metabolic EU Medical Device Regulations 2
F Definition Commercial Distribution - Definition - Scope of Commercial Distribution Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 2
P Definition Business Type - Definition of what we do-Business Type Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 4
E Brazil - RDC 183 - Finished device - Definition Question Other Medical Device Regulations World-Wide 1
B Warranty costs - What is your definition of a "warranty cost"? Nonconformance and Corrective Action 1

Similar threads

Top Bottom