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AUTOBIO Wash Buffer - Indonesia BPOM Medical Device Registration

AUTOBIO Wash Buffer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304918568. The device is manufactured by AUTOBIO DIAGNOSTICS CO.,LTD from China, and is classified as Risk Class Kelas Resiko : A. 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.

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BPOM Registered
Risk Class Kelas Resiko : A
AUTOBIO Wash Buffer
Analysis ID: AKL 20304918568

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

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

Mar 15, 2024

Expiry Date

Jun 01, 2026

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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DJ Fang

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