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KOFA GGT Reagent Kit - Indonesia BPOM Medical Device Registration

KOFA GGT Reagent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101322499. The device is manufactured by GUANGZHOU KOFA BIOTECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOLAB ARTHA MEDIKA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
KOFA GGT Reagent Kit
Analysis ID: AKL 20101322499

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INDOLAB ARTHA MEDIKA

AR Address

Komp Ruko Sunter Paradise Tahap II Blok.A4 No.43. Sunter Agung Podomoro

Registration Date

Feb 10, 2023

Expiry Date

Mar 06, 2027

Product Type

Clinical Chemistry Test System

Gamma-glutamyl transpeptidase and isoenzymes test system (strip & midstream)

Invitro Diagnostics

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