Identity
- Trade Name
- Clear Cannula FDA UDI
- Generic Name
- Hand ligament surgical release instrument FDA UDI
- Device Name
- 4mm Clear Cannula for Endoscopic CTR/CuTR FDA UDI
- Model / Reference
- 9600-22 FDA UDI
- Description
- 4mm Clear Cannula for Endoscopic CTR/CuTR FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00857915007484 FDA UDI
- FDA Product Code
- NBH FDA UDI
- GMDN Term
- Hand ligament surgical release instrument 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Hand ligament surgical release instrument
Clear Cannula by A.m. Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Hand ligament surgical release instrument.
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
- A.m. Surgical, Inc.
Sources (1)
- FDA UDI 74b419f3-81ea-43b4-a951-d0ad22eeb2ba 34 fields · synced May 30, 2026