ISO 13485
Identification and Traceability Register
Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements.
Fully Customizable
Audit Ready
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- Standard
- ISO 13485
- Document Type
- Register
- Format
- DOCX
- Language
- English
- Tags
- ISO 13485, Medical Devices, Register
This register defines how product is identified and records the links needed to trace finished devices back to their materials, processes and records, and forward to the customers who received them.
What's Inside
- Identification Scheme
- UDI Structure (GS1)
- Status Identification
- Backward Traceability — Finished Lot to Materials and Records
- Forward Traceability — Distribution Records
- Traceability Test (Mock Recall)
- Traceability Requirements by Market
- Register Review
ISO 13485 Alignment
Supports ISO 13485:2016 requirements, including Clauses 7.5.8 and 7.5.9.1. It fits with the rest of the QEHS Vault ISO 13485 document set.
Format
Supplied as a fully editable Microsoft Word (.docx) file. Add your organisation’s name, logo and details, then use it straight away. Instant download after purchase.
Key Benefits
- Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements
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