Identity
- Trade Name
- CODMAN FDA UDI
- Generic Name
- Scalp clip forceps FDA UDI
- Device Name
- CODMAN Scalp Clip Removal Forceps FDA UDI
- Model / Reference
- 20-1039 FDA UDI
- Description
- CODMAN Scalp Clip Removal Forceps FDA UDI
Identifiers
- Catalog Number
- 201039 FDA UDI
- Primary DI / UDI-DI
- 10886704001171 FDA UDI
- 510(k) Number
- K905433 FDA UDI
- FDA Product Code
- HBO FDA UDI
- GMDN Term
- Scalp clip forceps FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4150 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
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
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 edb6ecce-a7bc-463c-af63-170941072bfa 37 fields · synced Jun 6, 2026