Identity
- Trade Name
- TROTEC FDA UDI
- Generic Name
- Laparoscopic access cannula seal, reusable FDA UDI
- Device Name
- PROTECTIVE CAP reusable FDA UDI
- Model / Reference
- 8923991 FDA UDI
- Description
- PROTECTIVE CAP reusable FDA UDI
Identifiers
- Catalog Number
- 8923.991 FDA UDI
- Primary DI / UDI-DI
- 04055207001134 FDA UDI
- FDA Product Code
- FBQ FDA UDI
- GMDN Term
- Laparoscopic access cannula seal, 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
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 96c6d9ea-2ceb-4f3f-a7d4-b9f2582501f9 36 fields · synced Jun 6, 2026