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BriteMed Medical Monitor - Indonesia BPOM Medical Device Registration

BriteMed Medical Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801022519. The device is manufactured by BRITEMED TECHNOLOGY INC from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEGA GLOBAL PRATAMA.

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
BriteMed Medical Monitor
Analysis ID: AKL 20801022519

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

MEGA GLOBAL PRATAMA

AR Address

JL. Cengkeh Blok 16 No. 11 Kel. Pinangsia Kec. Tamansari Jakarta Barat 11110

Registration Date

May 02, 2020

Expiry Date

Oct 28, 2024

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories

Non Radiation Electromedics

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