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POLARIS® SPV ADJUSTABLE VALVE WITH ANTECHAMBER AND SiphonX®
EUDAMEDFDA UDIClass III (EU MDR)
Ref SPVA-SXRef SPV
by Sophysa
Identity
- Trade Name
- POLARIS® SPV ADJUSTABLE VALVE WITH ANTECHAMBER AND SiphonX® EUDAMEDPOLARIS® SPV ADJUSTABLE VALVE EUDAMEDSophysa FDA UDI
- Generic Name
- Cerebrospinal fluid shunt valve FDA UDI
- Device Name
- POLARIS® SPV ADJUSTABLE VALVE WITH ANTECHAMBER AND SiphonX® EUDAMEDPolaris® adjustable valve / 5 press. EUDAMEDPOLARIS ADJUSTABLE VALVE/5 PRESS. FDA UDIPOLARIS ADJUSTABLE VALVE, 30-200 WITH ANTECHAMBER AND SIPHONX FDA UDI
- Model / Reference
- SPVA-SX EUDAMEDFDA UDISPV EUDAMEDFDA UDI
- Description
- POLARIS ADJUSTABLE VALVE/5 PRESS. FDA UDIPOLARIS ADJUSTABLE VALVE, 30-200 WITH ANTECHAMBER AND SIPHONX FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03760124131710 EUDAMEDFDA UDI03760124131253 EUDAMEDFDA UDI
- Basic UDI-DI
- B-03760124131710 EUDAMEDB-03760124131253 EUDAMED
- FDA Product Code
- JXG FDA UDI
- EMDN Code
- N01038099 INTRACRANIAL DRAINAGE DEVICES AND KITS - ACCESSORIES - OTHER EUDAMED
- GMDN Term
- Cerebrospinal fluid shunt valve FDA UDI
Classification
- Device Class
- Class III EUDAMEDClass II FDA UDI
- Regulation Number
- 882.5550 FDA UDI
- Market of Registration
- Spain EUDAMEDFrance EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
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
No
FDA UDI
MR Conditional FDA UDI
POLARIS® SPV ADJUSTABLE VALVE WITH ANTECHAMBER AND SiphonX® by Sophysa — Class III — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-03760124131710 | Class III | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Sophysa
- EUDAMED SRN
- FR-MF-000002870
Sources (4)
- EUDAMED f8e61ef8-4db2-47dc-bcbb-9504f486ebbd 61 fields · synced Jul 15, 2026
- FDA UDI fd7b5397-4289-46b5-9ac6-acc9a3014d5c 33 fields · synced May 29, 2026
- FDA UDI cfda3bca-5a94-46ec-8bc4-4a133872b046 33 fields · synced May 30, 2026
- EUDAMED 49f45bf7-76a0-4849-9c7a-11cedab959b7 61 fields · synced Jul 15, 2026