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ERBA GGT 100 - Indonesia BPOM Medical Device Registration

ERBA GGT 100 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101121926. The device is manufactured by ERBA LACHEMA S.R.O from Czech Republic, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ELBA LAB 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
ERBA GGT 100
Analysis ID: AKL 20101121926

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ERBA LACHEMA S.R.O

Country of Origin

Czech Republic

Authorized Representative

PT. ELBA LAB MEDIKA

AR Address

GRAHA BUMI INDAH LANTAI II ROOM 2005, JL. RAYA KALIMALANG KAV. AGRARIA NO. 8-0 RT/RW 002/016 KEL. DUREN SAWIT KEC. DUREN SAWIT JAKARTA TIMUR

Registration Date

Apr 07, 2021

Expiry Date

Sep 06, 2024

Product Type

Clinical Chemistry Test System

Gamma-glutamyl transpeptidase and isoenzymes test system (kit & cair)

Invitro Diagnostics

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