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Alinity

FDA UDI

Class II (US FDA UDI)

by Abbott

Identity

Trade Name
Alinity FDA UDI
Generic Name
Glucose IVD, kit, spectrophotometry FDA UDI
Device Name
Alinity c Glucose Reagent Kit FDA UDI
Model / Reference
07P5530 FDA UDI
Description
Alinity c Glucose Reagent Kit FDA UDI

Identifiers

Catalog Number
07P5530 FDA UDI
Primary DI / UDI-DI
00380740135454 FDA UDI
FDA Product Code
CFR FDA UDI
GMDN Term
Glucose IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 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: Glucose IVD, kit, spectrophotometry

Alinity by Abbott — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose IVD, kit, spectrophotometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott

Sources (1)

  • FDA UDI c6f6e9b7-8eb0-4c4f-a48f-5f3e8439792a 36 fields · synced May 30, 2026