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Gmate UTM (Universal Transport Medium) - Indonesia BPOM Medical Device Registration

Gmate UTM (Universal Transport Medium) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302220079. The device is manufactured by PHILOSYS, CO., LTD., from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BUDIMANMAJU MEGAH PHARMACY.

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 : A
Gmate UTM (Universal Transport Medium)
Analysis ID: AKL 10302220079

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Korea

Authorized Representative

PT. BUDIMANMAJU MEGAH PHARMACY

AR Address

BURSA EFEK INDONESIA TOWER I LANTAI 17 SUITE 1710, JL. JEND. SUDIRMAN KAV. 52-53

Registration Date

Jun 01, 2022

Expiry Date

Mar 07, 2024

Product Type

Microbiology Equipment

Transport culture medium.

Invitro Diagnostics

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