Alinity m

FDA UDI

Class II (US FDA UDI)

by Abbott Molecular

Identity

Trade Name: Alinity m FDA UDI
Generic Name: Test tube rack FDA UDI
Device Name: Alinity m Universal Sample Rack FDA UDI
Model / Reference: 09N26-016 FDA UDI
Description: Alinity m Universal Sample Rack FDA UDI

Identifiers

Catalog Number: 09N26-016 FDA UDI
Primary DI / UDI-DI: 00884999047464 FDA UDI
FDA Product Code: OOI FDA UDI
GMDN Term: Test tube rack 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Test tube rack

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Abbott Molecular

Sources (1)

FDA UDI f8ca1eb4-1b9b-49ca-93d3-e682f5a74337 36 fields · synced Jun 6, 2026