VIDAMED Infusion Pump - Indonesia BPOM Medical Device Registration
VIDAMED Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902321593. The device is manufactured by SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD from 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
SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTDCountry of Origin
China
Authorized Representative
PT. ANDRA PRIMA JAYAAR Address
JL. TANAH ABANG III NO. 19E KEL. PETOJO SELATAN KEC. GAMBIR
Registration Date
Feb 07, 2023
Expiry Date
Feb 02, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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