Identity
- Trade Name
- CODMAN FDA UDI
- Generic Name
- Intracerebral cannula, nonimplantable, reusable FDA UDI
- Device Name
- CODMAN D'ERRICO Ventricular Needle FDA UDI
- Model / Reference
- 45-1085 FDA UDI
- Description
- CODMAN D'ERRICO Ventricular Needle FDA UDI
Identifiers
- Catalog Number
- 451085 FDA UDI
- Primary DI / UDI-DI
- 10886704015796 FDA UDI
- FDA Product Code
- HAO FDA UDI
- GMDN Term
- Intracerebral cannula, nonimplantable, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 882.4535 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
Yes
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 I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Cerenovus, Inc.
Sources (1)
- FDA UDI 143b4894-a2fe-4c31-a43b-bec90328cc11 36 fields · synced Jun 1, 2026