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HUGEMED Video Laryngoscope - Indonesia BPOM Medical Device Registration

HUGEMED Video Laryngoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403520063. The device is manufactured by SHENZHEN HUGEMED MEDICAL TECHNICAL DEVELOPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. AMPM HEALTHCARE 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 : A
HUGEMED Video Laryngoscope
Analysis ID: AKL 10403520063

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. AMPM HEALTHCARE INDONESIA

AR Address

Jl.Cengkeh Kav.16 No.29-30

Registration Date

Jan 22, 2025

Expiry Date

Oct 14, 2029

Product Type

Therapeutic Anesthesia Equipment

Rigid laryngoscope.

Non Radiation Electromedics

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