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Alinity m

FDA UDI

Class II (US FDA UDI)

by Abbott Molecular

Identity

Trade Name
Alinity m FDA UDI
Generic Name
Laboratory instrument/analyser application software IVD FDA UDI
Device Name
Alinity m Resp-4-Plex Application Specification File FDA UDI
Model / Reference
09N79-03A FDA UDI
Description
Alinity m Resp-4-Plex Application Specification File FDA UDI

Identifiers

Catalog Number
09N79-03A FDA UDI
Primary DI / UDI-DI
00884999049383 FDA UDI
510(k) Number
K241573 FDA UDI
FDA Product Code
QOF FDA UDI
GMDN Term
Laboratory instrument/analyser application software IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3981 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laboratory instrument/analyser application software IVD

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

Similar devices

Also classified as Laboratory instrument/analyser application software IVD.

Cleared under the same submission

K241573 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott Molecular

Sources (1)

  • FDA UDI 32a02e65-c9ac-44e4-a95c-cb831b2f3316 36 fields · synced May 29, 2026