Identity
- Trade Name
- CODMAN® HAKIM® FDA UDI
- Generic Name
- Ventriculoperitoneal shunt FDA UDI
- Device Name
- CODMAN® HAKIM® Programmable Valve Micro II Valve, with SIPHONGUARD' and Unitized SALMONRICKHAM Reservoir (Plastic Base) Reservoir arm length 18mm Programmable in steps of 10mm H2O (98 Pa). 30mm H2O to 200mm H2O (294 Pa - 1960 Pa) FDA UDI
- Model / Reference
- NS5031A FDA UDI
- Description
- CODMAN® HAKIM® Programmable Valve Micro II Valve, with SIPHONGUARD' and Unitized SALMONRICKHAM Reservoir (Plastic Base) Reservoir arm length 18mm Programmable in steps of 10mm H2O (98 Pa). 30mm H2O to 200mm H2O (294 Pa - 1960 Pa) FDA UDI
Identifiers
- Catalog Number
- NS5031A FDA UDI
- Primary DI / UDI-DI
- 10381780525080 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
No
FDA UDI
MR Conditional 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 |
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Manufacturer
- Manufacturer
- Integra LifeSciences Production Corporation
Sources (1)
- FDA UDI 4a63b309-2c3e-45a4-8c2d-bf9f6c7b2e3e 36 fields · synced Jun 9, 2026