← Back to catalogue

Alinity

FDA UDI

Class II (US FDA UDI)

by Abbott Ireland

Identity

Trade Name
Alinity FDA UDI
Generic Name
Free thyroxine (FT4) IVD, kit, chemiluminescent immunoassay FDA UDI
Device Name
Alinity i Free T4 Reagent Kit 1200 Tests FDA UDI
Model / Reference
07P7030 FDA UDI
Description
Alinity i Free T4 Reagent Kit 1200 Tests FDA UDI

Identifiers

Catalog Number
07P7030 FDA UDI
Primary DI / UDI-DI
00380740121822 FDA UDI
FDA Product Code
CEC FDA UDI
GMDN Term
Free thyroxine (FT4) IVD, kit, chemiluminescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1695 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: Free thyroxine (FT4) IVD, kit, chemiluminescent immunoassay

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

Similar devices

Also classified as Free thyroxine (FT4) IVD, kit, chemiluminescent immunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Abbott Ireland

Sources (1)

  • FDA UDI dd5dca41-e37c-4776-85c5-f1ebaa1b8bfa 36 fields · synced Jun 1, 2026