Identification by Sticker - Returned Product Identification Problem

R

Rosana

#1
The company I am working with makes different kinds of products. Most products are stamped with their # but a minority is not because the material (metal) is not appropriate for stamping. The solution was to label them but if it is a returned product they don't have this label. How can I work with this? Any ideas?

Rosana :confused:
 
Elsmar Forum Sponsor
R

ralphsulser

#2
Possibly a color code using a paint marker may work, you could put a different color dot on each of the metal parts. We use something similar.
 
R

Rosana

#3
Yes, it is a good idea to put a different color dot.

Now the identification for most of our products is Julian date-pod #. This way, when we have a returned product we know which line made the product and when. This is good for warranty claims.

Thanks
Rosana
 
Thread starter Similar threads Forum Replies Date
qualprod Controlled sticker for product identification? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 15
A Require, Sticker Sketch or Photo for using as Identification of In-Process Materials Inspection, Prints (Drawings), Testing, Sampling and Related Topics 1
T ISO 9001 8.5.2. - Identification and traceability to Identify Outputs - Services ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
K Identification of hazards and Risk file IEC 62366 - Medical Device Usability Engineering 7
M Medical Device Identification & Codes - Article 27 Requirements questions EU Medical Device Regulations 1
T Non conformance product identification and traceability 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
qualprod Monitoring of lead time - Good KPI identification? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 14
Watchcat Identification of Test Sample in Test Reports? Design and Development of Products and Processes 22
B Marking of Medical Electrical equipment and accessories - Cl. 7.2.2 "Identification" and Cl. 7.2.4 "Accessories" IEC 60601 - Medical Electrical Equipment Safety Standards Series 4
M Informational EU – Unique Device Identification (UDI) System – FAQs Medical Device and FDA Regulations and Standards News 0
S ISO 14971 Risk Management - Questions for Hazard identification ISO 14971 - Medical Device Risk Management 2
Z Two Payment Identification Number (PIN) for the same order in DFUF website 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
K Identification and Traceability with an ERP system - Barcode Labels? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
M MDR Annex IX Chapter I, 2.2 (c) - Device identification procedures during manufacture. EU Medical Device Regulations 1
M Informational USFDA final guidance – Unique Device Identification: Convenience Kits Medical Device and FDA Regulations and Standards News 0
Stefan Mundt ISO 9001:2015 - 8.5.2 Identification and Traceability Manufacturing and Related Processes 14
S Looking for procedure on UDI (Unique Device Identification) 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
S UDI (Unique Device Identification) Requirements for Remanufactured devices 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
B Quality Management System documentation identification Document Control Systems, Procedures, Forms and Templates 11
K Document Numbering (Identification) System Document Control Systems, Procedures, Forms and Templates 10
N Requirements for the identification and traceability of demo product for sales force US Food and Drug Administration (FDA) 1
M RFID (Radio Frequency Identification) Registration in Europe and in MENA countries EU Medical Device Regulations 1
qualprod Identification of Training Needs = People Performance? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
H European Pharmacopoeia First Identification Requirements Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 1
J Identification of gage blocks General Measurement Device and Calibration Topics 8
DeeDeeM IATF16949, clause 8.5.2.1 Identification and traceability-supplemental IATF 16949 - Automotive Quality Systems Standard 1
DeeDeeM IATF 16949 - Clause 8.5.2 Identification and Traceability IATF 16949 - Automotive Quality Systems Standard 7
Q ISO 9001 Cl. 8.5.2 and 8.5.4 - Identification in Products ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
M Measurement Equipment - Identification of Calibration Status General Measurement Device and Calibration Topics 25
J Customer Identification and Traceability in Manufacturing Plans Manufacturing and Related Processes 5
M Risk Identification and Risk Assessment for any Process - Is it necessary? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 22
Edward Reesor UDI (Unique Device Identification): HIBCC or GS1? ISO 13485:2016 - Medical Device Quality Management Systems 31
R Identification of Medical Devices in MDD 93/42 Certificate EU Medical Device Regulations 2
L Managing Finance Processes - Identification of Sub Processes ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
M Informational Is Identification of Risks and Opportunities required for QMS Processes? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 96
dubrizo Initial Supplier Identification, Review and Controls ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
H UDI (Unique Device Identification) Requirements for IVD Software EU Medical Device Regulations 2
A Receiving Goods Inwards - Identification Records and Data - Quality, Legal and Other Evidence 8
Pmarszal UDI (Unique Device Identification) Transition Period - Packaging Labeling Other US Medical Device Regulations 5
Q RFID (radio frequency identification) registration for Medical Device Other Medical Device Regulations World-Wide 6
B Class II Medical Device UDI (Unique Device Identification) Question(s) Other US Medical Device Regulations 8
A Is Risk Identification and Treatment a Process? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 25
D 820.120 UDI (Unique Device Identification) Labeling Verification Requirements Other US Medical Device Regulations 11
M Identification of Glass Instruments and Measurement Devices General Measurement Device and Calibration Topics 2
A Identification of Customer Property: Customer-Supplied Thumb Drives & Ext Hard Drives ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
Z Failure Mode Identification in PFMEA according to AIAG FMEA Rev.4 FMEA and Control Plans 6
M Reagent Status Identification - 7.4.3 Verification of Purchased Product ISO 13485:2016 - Medical Device Quality Management Systems 6
Gman2 Identification of Raw Material being used In-Process ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
M Identification and labeling medical device replacement system components Other Medical Device and Orthopedic Related Topics 12
L Identification of Inputs vs. Outputs in Design and Development (Section 7.3) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4

Similar threads

Top Bottom