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VIDAMED Neonatal Ventilator - Indonesia BPOM Medical Device Registration

VIDAMED Neonatal Ventilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403221002. The device is manufactured by SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANDRA PRIMA JAYA.

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 : C
VIDAMED Neonatal Ventilator
Analysis ID: AKL 20403221002

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ANDRA PRIMA JAYA

AR Address

JL. TANAH ABANG III NO. 19E KEL. PETOJO SELATAN KEC. GAMBIR

Registration Date

Dec 28, 2022

Expiry Date

Dec 27, 2025

Product Type

Therapeutic Anesthesia Equipment

Continuous ventilator.

Non Radiation Electromedics

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DJ Fang

DJ Fang

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