Identity
- Trade Name
- CODMAN® HAKIM® FDA UDI
- Generic Name
- Ventriculoperitoneal shunt FDA UDI
- Device Name
- CODMAN® HAKIM® Programmable Valve In-Line Valve and Unitized Distal Catheter Programmable in steps of 10mm H2O (98 Pa): 30mm H2O to 200mm H2O (294 Pa - 1960 Pa) FDA UDI
- Model / Reference
- 823844 FDA UDI
- Description
- CODMAN® HAKIM® Programmable Valve In-Line Valve and Unitized Distal Catheter Programmable in steps of 10mm H2O (98 Pa): 30mm H2O to 200mm H2O (294 Pa - 1960 Pa) FDA UDI
Identifiers
- Catalog Number
- 82-3844 FDA UDI
- Primary DI / UDI-DI
- 10381780519843 FDA UDI
- FDA Product Code
- JXG FDA UDI
- GMDN Term
- Ventriculoperitoneal shunt 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
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Catheter Length — 120 Centimeter FDA UDI
Category: Ventriculoperitoneal shunt
Codman® Hakim® by Integra LifeSciences Production Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ventriculoperitoneal shunt.
- StrataMR II — Medtronic PS Medical · Class II
- Strata®, BioGlide® — Medtronic PS Medical · Class II
- Integra® — Integra Lifesciences Corp. · Class II
- Novus™ — Integra Lifesciences Corp. · Class II
- Delta®, BioGlide® — Medtronic PS Medical · Class II
- Strata® — Medtronic PS Medical · Class II
- Strata™ — Medtronic PS Medical · Class II
- Delta® — Medtronic PS Medical · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Integra LifeSciences Production Corporation
Sources (1)
- FDA UDI 50a01476-ce5a-4ab4-8696-21cad716938e 37 fields · synced Jun 9, 2026