Identity
- Trade Name
- ALYX Plasma Kit FDA UDI
- Generic Name
- Apheresis system tubing set FDA UDI
- Device Name
- For Collection of Plasma Product by Centrifugation. For Use With the ALYX System. Sterile Fluid Path. FDA UDI
- Model / Reference
- 4R5730 FDA UDI
- Description
- For Collection of Plasma Product by Centrifugation. For Use With the ALYX System. Sterile Fluid Path. FDA UDI
Identifiers
- Catalog Number
- 4R5730 FDA UDI
- Primary DI / UDI-DI
- 00811137012916 FDA UDI
- FDA Product Code
- GKT FDA UDI
- GMDN Term
- Apheresis system tubing set FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.9245 FDA UDI
- Commercial Distribution
- Not 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
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
ALYX Plasma Kit by Fenwal, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
BK130030 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
- Fenwal, Inc.
Sources (1)
- FDA UDI 6d84b13a-cbed-4e59-b69a-e1477129756c 37 fields · synced May 30, 2026