Pure Global

REIGED DIAGNOSTICS EDTA-K3 Tube Vacuum Blood Collection Tube - Indonesia BPOM Medical Device Registration

REIGED DIAGNOSTICS EDTA-K3 Tube Vacuum Blood Collection Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101714162. The device is manufactured by SHANDONG CHENGWU MEDICAL PRODUCTS FACTORY. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. RAJAERBA INDOCHEM.

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
REIGED DIAGNOSTICS EDTA-K3 Tube Vacuum Blood Collection Tube
Analysis ID: AKL 20101714162

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. RAJAERBA INDOCHEM

AR Address

GEDUNG PEMBINA GRAHA JL. DI. PANJAITAN NO.45 RAWA BUNGA

Registration Date

May 06, 2021

Expiry Date

May 05, 2024

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