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Spotchem™ Ii Ggt

FDA UDI

Class I (US FDA UDI)

by Arkray Usa, Inc.

Identity

Trade Name
SPOTCHEM™ II GGT FDA UDI
Generic Name
Magnesium (Mg2+) IVD, kit, spectrophotometry FDA UDI
Device Name
Strip description for the invitro quantitative determination of GGT (y-glutamyltransferase or y-glutamyl tanspeptidase, (Y-GPT) activity in human plasma from whole blood samples FDA UDI
Model / Reference
77114 FDA UDI
Description
Strip description for the invitro quantitative determination of GGT (y-glutamyltransferase or y-glutamyl tanspeptidase, (Y-GPT) activity in human plasma from whole blood samples FDA UDI

Identifiers

Primary DI / UDI-DI
00015482771140 FDA UDI
FDA Product Code
JPZ FDA UDI
GMDN Term
Magnesium (Mg2+) IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1360 FDA UDI
Commercial Distribution
Not 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

Spotchem™ Ii Ggt by Arkray Usa, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Arkray Usa, Inc.

Sources (1)

  • FDA UDI b6757553-2c05-42ef-b6a7-2806aa2af83a 36 fields · synced May 30, 2026