Identity
- Trade Name
- CODMAN FDA UDI
- Generic Name
- Aneurysm clip FDA UDI
- Device Name
- CODMAN Slimline Mini Aneurysm Clip No 7 Bayonet 6mm FDA UDI
- Model / Reference
- 20-1833 FDA UDI
- Description
- CODMAN Slimline Mini Aneurysm Clip No 7 Bayonet 6mm FDA UDI
Identifiers
- Catalog Number
- 201833 FDA UDI
- Primary DI / UDI-DI
- 10886704002314 FDA UDI
- 510(k) Number
- K091921 FDA UDI
- FDA Product Code
- HCH FDA UDI
- GMDN Term
- Aneurysm clip FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5200 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
No
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
MR Conditional FDA UDI
Codman by Cerenovus, Inc. — 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
- Cerenovus, Inc.
Sources (1)
- FDA UDI 21cd5e0c-2155-48c8-ae9a-ecb3c414716d 37 fields · synced May 31, 2026