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.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VADI MEDICAL TECHNOLOGY CO., LTD. YANGMEICountry of Origin
Taiwan (China)
Authorized Representative
PT. ANDRA PRIMA JAYAAR 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.
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