VIDA Feeding Tube - Indonesia BPOM Medical Device Registration
VIDA Feeding Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805520041. The device is manufactured by WELL LEAD MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DANVI MEDILAB PERKASA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WELL LEAD MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. DANVI MEDILAB PERKASAAR Address
Jl. Kapten Muslim Komp. Mega Com Center Blok G No. 1-2 Kel. Dwikora Kec. Medan Helvetia
Registration Date
Jan 30, 2025
Expiry Date
Jan 29, 2028
Product Type
Therapeutic Gastroenterology-Urology Equipment
Gastrointestinal tube and accessories.
Non Electromedic Sterile
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