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Alinity

FDA UDI

Class II (US FDA UDI)

by Abbott Laboratories, Inc.

Identity

Trade Name
Alinity FDA UDI
Generic Name
C-reactive protein (CRP) IVD, calibrator FDA UDI
Device Name
Alinity c CRP Vario High Sensitivity Calibrator Kit FDA UDI
Model / Reference
07P5604 FDA UDI
Description
Alinity c CRP Vario High Sensitivity Calibrator Kit FDA UDI

Identifiers

Catalog Number
07P5604 FDA UDI
Primary DI / UDI-DI
00380740180348 FDA UDI
FDA Product Code
JIS FDA UDI
GMDN Term
C-reactive protein (CRP) IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 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: C-reactive protein (CRP) IVD, calibrator

Alinity by Abbott Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as C-reactive protein (CRP) IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9eaa002e-f374-44bf-97bc-9bfd0dd44e79 36 fields · synced May 29, 2026