Identity
- Trade Name
- Alinity FDA UDI
- Generic Name
- Lithium therapeutic drug monitoring IVD, reagent FDA UDI
- Device Name
- Alinity c Lithium Reagent Kit 190 Tests FDA UDI
- Model / Reference
- 08P5320 FDA UDI
- Description
- Alinity c Lithium Reagent Kit 190 Tests FDA UDI
Identifiers
- Catalog Number
- 08P5320 FDA UDI
- Primary DI / UDI-DI
- 00380740136277 FDA UDI
- FDA Product Code
- NDW FDA UDI
- GMDN Term
- Lithium therapeutic drug monitoring IVD, reagent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3560 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Category: Lithium therapeutic drug monitoring IVD, reagent
Alinity by Abbott Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Diazyme — Diazyme Laboratories, Inc.
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- Thermo Scientific Infinity™ — Fisher Diagnostics · Class II
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
- Abbott Laboratories, Inc.
Sources (1)
- FDA UDI 8989443f-46b1-4e04-8a65-2dbae5879e34 36 fields · synced May 31, 2026