Identity
- Trade Name
- TROTEC FDA UDI
- Generic Name
- Laparoscopic access cannula, reusable FDA UDI
- Device Name
- SHEATH W. TROCAR TIP SZ 10MM WL 181MM distal tip conical, with automatic protection function, reusable FDA UDI
- Model / Reference
- 8923132 FDA UDI
- Description
- SHEATH W. TROCAR TIP SZ 10MM WL 181MM distal tip conical, with automatic protection function, reusable FDA UDI
Identifiers
- Catalog Number
- 8923.132 FDA UDI
- Primary DI / UDI-DI
- 04055207022443 FDA UDI
- FDA Product Code
- FBQ FDA UDI
- GMDN Term
- Laparoscopic access cannula, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5090 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 181 Millimeter FDA UDI
Trotec by Richard Wolf GmbH — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Richard Wolf GmbH
Sources (1)
- FDA UDI b84a34f4-4f60-40da-bf4f-4c16a57515e2 37 fields · synced Jun 7, 2026