Identity
- Trade Name
- Sophysa FDA UDI
- Generic Name
- Cerebrospinal fluid reservoir FDA UDI
- Device Name
- IN LINE CSF RES.DOUBLE DOME / CATH FDA UDI
- Model / Reference
- RE-1241 FDA UDI
- Description
- IN LINE CSF RES.DOUBLE DOME / CATH FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03760124130850 FDA UDI
- 510(k) Number
- K013488 FDA UDI
- FDA Product Code
- JXG FDA UDI
- GMDN Term
- Cerebrospinal fluid reservoir 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
No
FDA UDI
Contains Latex
No
FDA UDI
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
Yes
FDA UDI
MR Safe FDA UDI
Category: Cerebrospinal fluid reservoir
Sophysa by Sophysa SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cerebrospinal fluid reservoir.
- Sophysa — Sophysa SA · Class II
- Sophysa — Sophysa SA · Class II
- Sophysa — Sophysa SA · Class II
- Sophysa — Sophysa SA · Class II
- Sophysa — Sophysa SA · Class II
- Sophysa — Sophysa SA · Class II
- Sophysa — Sophysa SA · Class II
- Sophysa — Sophysa SA · Class II
Cleared under the same submission
K013488 also covers:
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
- Sophysa SA
Sources (1)
- FDA UDI e86e4b7e-d5e7-47d4-8b8a-a8ac1e87c72b 34 fields · synced Jun 1, 2026