Pure Global

Bruker MALDI Biotyper-BD Sirius IVD System - Indonesia BPOM Medical Device Registration

Bruker MALDI Biotyper-BD Sirius IVD System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220358. The device is manufactured by BRUKER DALTONICS GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BECTON DICKINSON INDONESIA.

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
Bruker MALDI Biotyper-BD Sirius IVD System
Analysis ID: AKL 20303220358

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. BECTON DICKINSON INDONESIA

AR Address

SAMPOERNA STRATEGIC SQUARE, SOUTH TOWER LT.20 JL. JEND SUDIRMAN KAV 45-46

Registration Date

Jan 27, 2024

Expiry Date

Feb 25, 2025

Product Type

Serological Reagents

Mass spectrometer system for clinical use for the identification of microorganism

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from BRUKER DALTONICS GMBH & CO. KG.
Products from the same manufacturer (1 products)