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DUMOLAB Anti-AB, Monoclonal - Indonesia BPOM Medical Device Registration

DUMOLAB Anti-AB, Monoclonal is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209520016. The device is manufactured by DIALAB GES.M.B.H from Austria, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. LABORA DIAGNOSTIC PARTNERS.

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 : C
DUMOLAB Anti-AB, Monoclonal
Analysis ID: AKL 20209520016

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

DIALAB GES.M.B.H

Country of Origin

Austria

Authorized Representative

PT. LABORA DIAGNOSTIC PARTNERS

AR Address

MITRA DIAGNOSTIK LABORA

Registration Date

Jan 13, 2025

Expiry Date

Jan 12, 2026

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Automated blood grouping and antibody test system.

Invitro Diagnostics

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