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VIDAMED Respiratory Humidifier - Indonesia BPOM Medical Device Registration

VIDAMED Respiratory Humidifier is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403220563. The device is manufactured by VADI MEDICAL TECHNOLOGY CO., LTD. YANGMEI from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. 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 : B
VIDAMED Respiratory Humidifier
Analysis ID: AKL 20403220563

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. ANDRA PRIMA JAYA

AR Address

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

Registration Date

Aug 16, 2022

Expiry Date

Aug 03, 2025

Product Type

Therapeutic Anesthesia Equipment

Respiratory gas humidifier.

Non Radiation Electromedics

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