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Pointe GGT Reagent

FDA UDI

Class I (US FDA UDI)

by Pointe Scientific, Inc.

Identity

Trade Name
Pointe GGT Reagent FDA UDI
Generic Name
Gamma-glutamyltransferase (GGT) IVD, reagent FDA UDI
Device Name
Pointe GGT Reagent packaged for use on the Mindray BA800. 4 x 42ml R1, 4 x 17ml R2. For the quantitative kinetic determination of gamma glutamyl transferase (gGT) activity in serum. For in vitro diagnostic use only. FDA UDI
Model / Reference
16-HG959-236 FDA UDI
Description
Pointe GGT Reagent packaged for use on the Mindray BA800. 4 x 42ml R1, 4 x 17ml R2. For the quantitative kinetic determination of gamma glutamyl transferase (gGT) activity in serum. For in vitro diagnostic use only. FDA UDI

Identifiers

Catalog Number
16-HG959-236 FDA UDI
Primary DI / UDI-DI
00811727016140 FDA UDI
510(k) Number
K973157 FDA UDI
FDA Product Code
JQB FDA UDI
GMDN Term
Gamma-glutamyltransferase (GGT) IVD, reagent 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

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

No

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, reagent

Pointe GGT Reagent by Pointe Scientific, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1b59305d-ec52-4fbf-8319-96d19f4a4a22 37 fields · synced Jun 8, 2026