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GLOTECH Laboratory Incubator - Indonesia BPOM Medical Device Registration

GLOTECH Laboratory Incubator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302912490. The device is manufactured by ZENITH LAB (JIANGSU) CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GLOMED ADINATA PRIMA.

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
GLOTECH Laboratory Incubator
Analysis ID: AKL 10302912490

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. GLOMED ADINATA PRIMA

AR Address

Jl. Gunung Sahari Raya No.2 Blok E/23-A Kelurahan : Pademangan Barat Kecamatan : Pademangan

Registration Date

Mar 16, 2022

Expiry Date

Mar 16, 2025

Product Type

Microbiology Equipment

Microbiological incubator.

Invitro Diagnostics

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