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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
Molecular grade buffered sample diluent IVD FDA UDI
Device Name
Alinity m Diluent Solution Kit FDA UDI
Model / Reference
09N20-003 FDA UDI
Description
Alinity m Diluent Solution Kit FDA UDI

Identifiers

Catalog Number
09N20-003 FDA UDI
Primary DI / UDI-DI
00884999047907 FDA UDI
FDA Product Code
OOI FDA UDI
GMDN Term
Molecular grade buffered sample diluent IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.2570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: Molecular grade buffered sample diluent IVD

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

Similar devices

Also classified as Molecular grade buffered sample diluent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott Molecular

Sources (1)

  • FDA UDI bb9e3de0-567a-4fb7-a292-c14e00c1563a 36 fields · synced Jun 1, 2026