Identity
- Trade Name
- CODMAN® HOLTER® FDA UDI
- Generic Name
- Cerebrospinal fluid shunt connector FDA UDI
- Device Name
- CODMAN® HOLTER® Type B Fixation and Joining Connector Straight FDA UDI
- Model / Reference
- 821695 FDA UDI
- Description
- CODMAN® HOLTER® Type B Fixation and Joining Connector Straight FDA UDI
Identifiers
- Catalog Number
- 82-1695 FDA UDI
- Primary DI / UDI-DI
- 10381780515531 FDA UDI
- FDA Product Code
- JXG FDA UDI
- GMDN Term
- Cerebrospinal fluid shunt connector FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5550 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Conditional FDA UDI
Category: Cerebrospinal fluid shunt connector
Codman® Holter® by Integra LifeSciences Production Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Integra LifeSciences Production Corporation
Sources (1)
- FDA UDI f6d2ccdc-6a73-4e19-bedd-664aeaa61d5b 36 fields · synced Jun 9, 2026