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MEDLAB Capnograph - Indonesia BPOM Medical Device Registration

MEDLAB Capnograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502320638. The device is manufactured by MEDLAB MEDIZINISCHE DIAGNOSEGERATE GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FA ANTARES MEDIKA.

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
MEDLAB Capnograph
Analysis ID: AKL 20502320638

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. FA ANTARES MEDIKA

AR Address

RUKO GOLDEN BOULEVARD BLOK I NO.7

Registration Date

Jan 14, 2025

Expiry Date

Jan 01, 2027

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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