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Alinity

FDA UDI

Class II (US FDA UDI)

by Abbott

Identity

Trade Name
Alinity FDA UDI
Generic Name
Hepatitis A virus immunoglobulin G (IgG) antibody IVD, calibrator FDA UDI
Device Name
HAVAb IgG II Calibrator FDA UDI
Model / Reference
06S9301 FDA UDI
Description
HAVAb IgG II Calibrator FDA UDI

Identifiers

Catalog Number
06S9301 FDA UDI
Primary DI / UDI-DI
00380740197636 FDA UDI
510(k) Number
K222850 FDA UDI
FDA Product Code
JIS FDA UDI
GMDN Term
Hepatitis A virus immunoglobulin G (IgG) antibody IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 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: Hepatitis A virus immunoglobulin G (IgG) antibody IVD, calibrator

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

Similar devices

Also classified as Hepatitis A virus immunoglobulin G (IgG) antibody IVD, calibrator.

Cleared under the same submission

K222850 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott

Sources (1)

  • FDA UDI cdd7d26b-ff07-45b3-81d3-90d0b5e9fe95 37 fields · synced Jun 8, 2026