Identity
- Trade Name
- CODMAN HAKIM SIPHONGUARD RICKHAM FDA UDI
- Generic Name
- Ventriculoperitoneal shunt FDA UDI
- Device Name
- CODMAN HAKIM Programmable Valve Micro II Valve, with SIPHONGUARD and Unitized SALMON-RICKHAM Reservoir (Plastic Base) Reservoir arm length 18mm Programmable in steps of 10mm H2O (98 Pa): 30mm H2O to 200mm H2O (294 Pa - 1960 Pa) Includes: Ventricular Catheter 14cm, Stylet, Peritoneal Catheter 120cm, Priming Adapter and Information Manual FDA UDI
- Model / Reference
- NS5031A FDA UDI
- Description
- CODMAN HAKIM Programmable Valve Micro II Valve, with SIPHONGUARD and Unitized SALMON-RICKHAM Reservoir (Plastic Base) Reservoir arm length 18mm Programmable in steps of 10mm H2O (98 Pa): 30mm H2O to 200mm H2O (294 Pa - 1960 Pa) Includes: Ventricular Catheter 14cm, Stylet, Peritoneal Catheter 120cm, Priming Adapter and Information Manual FDA UDI
Identifiers
- Catalog Number
- NS5031A FDA UDI
- Primary DI / UDI-DI
- 10886704046622 FDA UDI
- 510(k) Number
- K091346 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
- Not 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
Codman Hakim Siphonguard Rickham 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 90803068-22e6-4f14-b79c-196e97a40a35 37 fields · synced Jun 8, 2026