Identity
- Trade Name
- PATHWAY FDA UDI
- Generic Name
- Orthopaedic implant/instrument dismantling device FDA UDI
- Device Name
- PATHWAY DISASSEMBLY DRIVER FDA UDI
- Model / Reference
- 1299-01-030 FDA UDI
- Description
- PATHWAY DISASSEMBLY DRIVER FDA UDI
Identifiers
- Catalog Number
- 129901030 FDA UDI
- Primary DI / UDI-DI
- 10603295026860 FDA UDI
- FDA Product Code
- HXX FDA UDI
- GMDN Term
- Orthopaedic implant/instrument dismantling device FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Pathway by Depuy International Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Depuy International Ltd
Sources (1)
- FDA UDI 2bc5251e-135a-47fc-9ad8-683d29d2c4ce 36 fields · synced Jun 8, 2026