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HEMI Video Bronchoscope series - Indonesia BPOM Medical Device Registration

HEMI Video Bronchoscope series is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20703420145. The device is manufactured by SONOSCAPE MEDICAL CORP from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HOSPI MEDIK 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
HEMI Video Bronchoscope series
Analysis ID: AKL 20703420145

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. HOSPI MEDIK INDONESIA

AR Address

Gedung Indra Sentral Blok E-F Lantai 1-2 Jl. Letjen Suprapto No. 60 Kel. Cempaka Putih Barat Kec. Cempaka Putih, Jakarta Pusat 10520

Registration Date

Dec 30, 2024

Expiry Date

Apr 22, 2027

Product Type

Ear, Nose and Throat Surgical Equipment

Bronchoscope (flexible or rigid) and accessories.

Non Radiation Electromedics

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