Identity
- Trade Name
- CODMAN CERTAS SIPHONGUARD FDA UDI
- Generic Name
- Ventriculo-peritoneal/atrial shunt FDA UDI
- Device Name
- CODMAN CERTAS SIPHONGUARD Plus Programmable Valve Right Angle Valve with SIPHONGUARD, Accessories and Unitized Catheter Includes: Ventricular Catheter, Unitized Distal Catheter, Priming Adapter and Information Manual FDA UDI
- Model / Reference
- 82-8826PL FDA UDI
- Description
- CODMAN CERTAS SIPHONGUARD Plus Programmable Valve Right Angle Valve with SIPHONGUARD, Accessories and Unitized Catheter Includes: Ventricular Catheter, Unitized Distal Catheter, Priming Adapter and Information Manual FDA UDI
Identifiers
- Catalog Number
- 828826PL FDA UDI
- Primary DI / UDI-DI
- 10886704082033 FDA UDI
- FDA Product Code
- JXG FDA UDI
- GMDN Term
- Ventriculo-peritoneal/atrial 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 Certas Siphonguard by Medos International Sàrl — 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
- Medos International Sàrl
Sources (1)
- FDA UDI f95e0156-ef0d-4dc1-8e33-946c9c42b611 36 fields · synced May 31, 2026