Pure Global

AUTOBIO Tumor Marker Control II Level 1 - Indonesia BPOM Medical Device Registration

AUTOBIO Tumor Marker Control II Level 1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101120227. The device is manufactured by AUTOBIO DIAGNOSTICS CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GRACIA VISI 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
AUTOBIO Tumor Marker Control II Level 1
Analysis ID: AKL 20101120227

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GRACIA VISI PRATAMA

AR Address

Jl. Soekarno Hatta No. 8A, Kel. Tlogosari Kulon, Kec. Pedurungan, Kota Semarang

Registration Date

Jan 12, 2021

Expiry Date

Mar 20, 2025

Product Type

Clinical Chemistry Test System

Quality control material (assayed and unassayed) (cair)

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing