Identity
- Trade Name
- Alinity FDA UDI
- Generic Name
- Lactate IVD, kit, reduction/oxidation FDA UDI
- Device Name
- Alinity c Lactic Acid Reagent Kit 1000 Tests FDA UDI
- Model / Reference
- 08P2121 FDA UDI
- Description
- Alinity c Lactic Acid Reagent Kit 1000 Tests FDA UDI
Identifiers
- Catalog Number
- 08P2121 FDA UDI
- Primary DI / UDI-DI
- 00380740179199 FDA UDI
- FDA Product Code
- KHP FDA UDI
- GMDN Term
- Lactate IVD, kit, reduction/oxidation FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1450 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Lactate IVD, kit, reduction/oxidation
Alinity by Abbott — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Lactate IVD, kit, reduction/oxidation.
- ARCHITECT — Abbott Laboratories, Inc. · Class I
- Alinity — Abbott · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Abbott
Sources (1)
- FDA UDI b9d76467-f5fc-4014-8539-dea645186d3c 36 fields · synced May 30, 2026