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GD Vacuum Tube Sterile Plain - Indonesia BPOM Medical Device Registration

GD Vacuum Tube Sterile Plain is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101901928. 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. FAITHFUL MEDICAL GRACE.

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
GD Vacuum Tube Sterile Plain
Analysis ID: AKL 20101901928

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FAITHFUL MEDICAL GRACE

AR Address

Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89

Registration Date

May 01, 2021

Expiry Date

Oct 08, 2025

Product Type

Clinical Chemistry Test System

Blood specimen collection device

Invitro Diagnostics

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