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Idg/Sanzay

FDA UDI

Class I (US FDA UDI)

by IDG/SANZAY Corporation

Identity

Trade Name
IDG/SANZAY FDA UDI
Generic Name
Alanine aminotransferase (ALT) IVD, reagent FDA UDI
Device Name
For the quantitative determination of alanine aminotransferase in serum used in routine examination and monitoring of therapy and relapses. FDA UDI
Model / Reference
1 FDA UDI
Description
For the quantitative determination of alanine aminotransferase in serum used in routine examination and monitoring of therapy and relapses. FDA UDI

Identifiers

Catalog Number
C045 FDA UDI
Primary DI / UDI-DI
00850053916021 FDA UDI
FDA Product Code
CKA FDA UDI
GMDN Term
Alanine aminotransferase (ALT) IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1030 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

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

Dimensions & Sizes

Size
Total Volume — 100 Milliliter FDA UDI
Total Volume — 50 Milliliter FDA UDI
Total Volume — 120 Milliliter FDA UDI
Total Volume — 125 Milliliter FDA UDI
Total Volume — 1 Liter FDA UDI
Total Volume — 240 Milliliter FDA UDI
Total Volume — 250 Milliliter FDA UDI
Total Volume — 500 Milliliter FDA UDI

Category: Alanine aminotransferase (ALT) IVD, reagent

Idg/Sanzay by IDG/SANZAY Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alanine aminotransferase (ALT) IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI de95f78a-4a13-4f4f-bec2-364df62b2676 36 fields · synced May 30, 2026