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GP Vacu Tube Glucose - Indonesia BPOM Medical Device Registration

GP Vacu Tube Glucose is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101711153. The device is manufactured by ZHEJIANG GONGDONG MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GOLDEN PRATAMA.

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
GP Vacu Tube Glucose
Analysis ID: AKL 20101711153

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GOLDEN PRATAMA

AR Address

Puri Metropolitan Blok F7/12B, Petir, Cipondoh, Tangerang, Banten

Registration Date

Dec 01, 2020

Expiry Date

Nov 30, 2023

Product Type

Clinical Chemistry Test System

Blood specimen collection device

Invitro Diagnostics

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