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Yumizen C1200 GGT

FDA UDI

Class I (US FDA UDI)

by Horiba Abx

Identity

Trade Name
Yumizen C1200 GGT FDA UDI
Generic Name
Gamma-glutamyltransferase (GGT) IVD, kit, spectrophotometry FDA UDI
Model / Reference
1300023846 FDA UDI

Identifiers

Primary DI / UDI-DI
03610230006993 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

No

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

Yumizen C1200 GGT by Horiba Abx — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Horiba Abx

Sources (1)

  • FDA UDI 4eaa3b1c-8862-40b4-83d0-0236a52883ef 32 fields · synced Jun 8, 2026