← Back to catalogue

gamma-Glutamyltransferase ver.2 Standardized against IFCC / Szasz

FDA UDI

Class I (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
gamma-Glutamyltransferase ver.2 Standardized against IFCC / Szasz FDA UDI
Generic Name
Gamma-glutamyltransferase (GGT) IVD, kit, spectrophotometry FDA UDI
Model / Reference
5168775190 FDA UDI

Identifiers

Catalog Number
5168775190 FDA UDI
Primary DI / UDI-DI
04015630925018 FDA UDI
FDA Product Code
JQB FDA UDI
GMDN Term
Gamma-glutamyltransferase (GGT) IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1360 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Gamma-glutamyltransferase (GGT) IVD, kit, spectrophotometry

gamma-Glutamyltransferase ver.2 Standardized against IFCC / Szasz by Roche Diagnostics Corp. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Gamma-glutamyltransferase (GGT) IVD, kit, spectrophotometry.

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

Sources (1)

  • FDA UDI 0322080d-6f8f-4396-be79-157e441e8ff6 33 fields · synced May 30, 2026