Pure Global

CERTEST FOB - Indonesia BPOM Medical Device Registration

CERTEST FOB is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20206020614. The device is manufactured by CERTEST BIOTEC S.L from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MRK DIAGNOSTICS.

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
CERTEST FOB
Analysis ID: AKL 20206020614

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

CERTEST BIOTEC S.L

Country of Origin

Spain

Authorized Representative

PT. MRK DIAGNOSTICS

AR Address

JL. Merpati Mas I Blok B1 NO.46 Perkantoran Tanjung Mas Raya Tanjung Barat

Registration Date

Mar 21, 2022

Expiry Date

Jan 24, 2025

Product Type

Manual Hematology Equipment

Occult blood test

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing