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Alinity

FDA UDI

Class II (US FDA UDI)

by Abbott

Identity

Trade Name
Alinity FDA UDI
Generic Name
Human epididymis protein 4 (HE4) IVD, kit, chemiluminescent immunoassay FDA UDI
Device Name
Alinity i HE4 Reagent Kit 200 Tests FDA UDI
Model / Reference
08P5021 FDA UDI
Description
Alinity i HE4 Reagent Kit 200 Tests FDA UDI

Identifiers

Catalog Number
08P5021 FDA UDI
Primary DI / UDI-DI
00380740138349 FDA UDI
FDA Product Code
OIU FDA UDI
GMDN Term
Human epididymis protein 4 (HE4) IVD, kit, chemiluminescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.6010 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: Human epididymis protein 4 (HE4) IVD, kit, chemiluminescent immunoassay

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

Similar devices

Also classified as Human epididymis protein 4 (HE4) IVD, kit, chemiluminescent immunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott

Sources (1)

  • FDA UDI 83ad2594-313c-4999-b918-bc6bc13e5dc7 36 fields · synced Jun 1, 2026