Identity
- Trade Name
- T-FIX FDA UDI
- Generic Name
- Arthroscopic access cannula, single-use FDA UDI
- Device Name
- CANNULA KIT, 5.0 MM I.D. X 55 MM LONG, INCLUDES OBTURATOR AND TROCAR, STERILE, LATEX-FREE, BOX OF 10 FDA UDI
- Model / Reference
- 014623 FDA UDI
- Description
- CANNULA KIT, 5.0 MM I.D. X 55 MM LONG, INCLUDES OBTURATOR AND TROCAR, STERILE, LATEX-FREE, BOX OF 10 FDA UDI
Identifiers
- Catalog Number
- 014623 FDA UDI
- Primary DI / UDI-DI
- 03596010026040 FDA UDI
- FDA Product Code
- NBH FDA UDI
- GMDN Term
- Arthroscopic access cannula, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.1100 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Arthroscopic access cannula, single-use
T-Fix by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI 1f010464-11cd-4b92-98f1-1046622ada49 35 fields · synced Jun 8, 2026