Pure Global

GB Lab Vacuum Tube Plain Glass - Indonesia BPOM Medical Device Registration

GB Lab Vacuum Tube Plain Glass is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101520245. The device is manufactured by HEBEI XINLE SCI & TECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BERLIANTAMA DIAGNOSTIKA INDONESIA.

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 : B
GB Lab Vacuum Tube Plain Glass
Analysis ID: AKL 20101520245

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

BERLIANTAMA DIAGNOSTIKA INDONESIA

AR Address

JL.TAMAN SUNTER INDAH BLOK HJ2 NO.16

Registration Date

Feb 04, 2025

Expiry Date

Apr 24, 2027

Product Type

Clinical Chemistry Test System

Blood specimen collection device

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from BERLIANTAMA DIAGNOSTIKA INDONESIA
Products with the same authorized representative (2 products)