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Alinity

FDA UDI

Class I (US FDA UDI)

by Abbott

Identity

Trade Name
Alinity FDA UDI
Generic Name
Buffered sample diluent IVD FDA UDI
Device Name
Alinity h-series Diluent FDA UDI
Model / Reference
04R2601 FDA UDI
Description
Alinity h-series Diluent FDA UDI

Identifiers

Catalog Number
04R2601 FDA UDI
Primary DI / UDI-DI
00380740136024 FDA UDI
FDA Product Code
GIF FDA UDI
GMDN Term
Buffered sample diluent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.8200 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Buffered sample diluent IVD

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

Similar devices

Also classified as Buffered sample diluent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott

Sources (1)

  • FDA UDI eebe35d6-d0d0-4bff-b61e-28a3e6565645 36 fields · synced May 30, 2026