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BMC Polysomnograph - Indonesia BPOM Medical Device Registration

BMC Polysomnograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20402320082. The device is manufactured by BMC (TIANJIN) MEDICAL CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is WITH ALPHA 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.

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BPOM Registered
Risk Class Kelas Resiko : B
BMC Polysomnograph
Analysis ID: AKL 20402320082

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

WITH ALPHA INDONESIA

AR Address

Gedung Graha Sucofindo Lt, 10. Jl.Raya Pasar Minggu Kav.34, Rt.002/001, Kel Pancoran, Kec Pancoran, Kota Jakarta Selatan, Prov DKI Jakarta.

Registration Date

Apr 18, 2023

Expiry Date

Jul 02, 2027

Product Type

Monitoring Anesthesia Equipment

Apnea monitor.

Non Radiation Electromedics

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