Pure Global

GLOTECH Platelet Agitator - Indonesia BPOM Medical Device Registration

GLOTECH Platelet Agitator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209220182. The device is manufactured by ZENITH LAB (JIANGSU) CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
GLOTECH Platelet Agitator
Analysis ID: AKL 20209220182

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

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

Sep 05, 2022

Expiry Date

Sep 01, 2025

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Environmental chamber for storage of platelet concentrate.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing