Identity
- Trade Name
- Maky 21.1 FDA UDI
- Generic Name
- Haemodialysis dialyser reprocessing system FDA UDI
- Device Name
- Dialyzer reprocessing machine. FDA UDI
- Model / Reference
- 21.1 FDA UDI
- Description
- Dialyzer reprocessing machine. FDA UDI
Identifiers
- Catalog Number
- MAKY21.1 FDA UDI
- Primary DI / UDI-DI
- 00898021000037 FDA UDI
- 510(k) Number
- K024076 FDA UDI
- FDA Product Code
- LIF FDA UDI
- GMDN Term
- Haemodialysis dialyser reprocessing system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5820 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Haemodialysis dialyser reprocessing system
Maky 21.1 by Angelini Pharma Inc. — 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
- Angelini Pharma Inc.
Sources (1)
- FDA UDI 615b7242-ee00-4a02-aeec-5ed38c40b857 36 fields · synced Jun 9, 2026