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EUROIMMUN EUROBlotONE - Indonesia BPOM Medical Device Registration

EUROIMMUN EUROBlotONE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102220235. The device is manufactured by DYNEX TECHNOLOGIES SPOL. S R.O. from Czech Republic, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INTI MAKMUR MEDITAMA.

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
EUROIMMUN EUROBlotONE
Analysis ID: AKL 20102220235

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Czech Republic

Authorized Representative

PT. INTI MAKMUR MEDITAMA

AR Address

JL. SULTAN ISKANDAR MUDA, GANDARIA 8 OFFICE TOWER LANTAI 16 UNIT F, KEBAYORAN LAMA JAKARTA SELATAN

Registration Date

Sep 20, 2022

Expiry Date

Dec 31, 2024

Product Type

Clinical Laboratory Equipment

Discrete photometric chemistry analyzer for clinical use.

Invitro Diagnostics

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