Identity
- Trade Name
- Natus® FDA UDI
- Generic Name
- Lumboperitoneal shunt spinal catheter FDA UDI
- Device Name
- Y-LUMBAR CATHETER F5 FDA UDI
- Model / Reference
- NT951103 FDA UDI
- Description
- Y-LUMBAR CATHETER F5 FDA UDI
Identifiers
- Catalog Number
- NT951103 FDA UDI
- Primary DI / UDI-DI
- 00382830056250 FDA UDI
- 510(k) Number
- K944595 FDA UDI
- FDA Product Code
- JXG FDA UDI
- GMDN Term
- Lumboperitoneal shunt spinal catheter 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
Yes
FDA UDI
MR Safe FDA UDI
Category: Lumboperitoneal shunt spinal catheter
Natus® by Natus Medical Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Lumboperitoneal shunt spinal catheter.
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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
- Natus Medical Incorporated
Sources (1)
- FDA UDI e83baf0c-1ef7-45a0-ad6a-6ef9a9ea4e14 37 fields · synced May 31, 2026