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AMS Gamma GT - Indonesia BPOM Medical Device Registration

AMS Gamma GT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101323101. The device is manufactured by SCIENTIFIC MEDICAL PRODUCTS SUN. SAN. VE TIC. LTD.. STI from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TIRTA PASIFIK MEDIKATAMA.

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
AMS Gamma GT
Analysis ID: AKL 20101323101

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. TIRTA PASIFIK MEDIKATAMA

AR Address

JL. Jatibening Raya II, Ruko Jatibening No. 2 RT/RW 03/01

Registration Date

May 22, 2023

Expiry Date

May 21, 2026

Product Type

Clinical Chemistry Test System

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

Invitro Diagnostics

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