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VIMAC Video Laryngoscope - Indonesia BPOM Medical Device Registration

VIMAC Video Laryngoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403024709. The device is manufactured by HEBEI VIMED MEDICAL DEVICE, CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GAMAMED.

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
VIMAC Video Laryngoscope
Analysis ID: AKL 10403024709

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. GAMAMED

AR Address

JL. WR. SUPRATMAN 56 B

Registration Date

Aug 21, 2020

Expiry Date

May 22, 2025

Product Type

Therapeutic Anesthesia Equipment

Rigid laryngoscope.

Non Radiation Electromedics

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