← Back to catalogue

Architect

FDA UDI

Class II (US FDA UDI)

by Abbott

Identity

Trade Name
ARCHITECT FDA UDI
Generic Name
Total aspartate aminotransferase (AST) IVD, reagent FDA UDI
Device Name
Activated Aspartate Aminotransferase FDA UDI
Model / Reference
8L91-22 FDA UDI
Description
Activated Aspartate Aminotransferase FDA UDI

Identifiers

Catalog Number
08L9122 FDA UDI
Primary DI / UDI-DI
00380740161835 FDA UDI
FDA Product Code
CIT FDA UDI
GMDN Term
Total aspartate aminotransferase (AST) IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1100 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

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: Total aspartate aminotransferase (AST) IVD, reagent

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

Similar devices

Also classified as Total aspartate aminotransferase (AST) IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Abbott

Sources (1)

  • FDA UDI 913ec749-75db-4de7-ae3d-0d2025a29619 36 fields · synced May 30, 2026