AXIMED Rectal Tube - Indonesia BPOM Medical Device Registration
AXIMED Rectal Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805911912. The device is manufactured by JIANGSU WEIKANG JIEJING MEDICAL APPARATUS CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIO AXION HEALTHINDO.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. BIO AXION HEALTHINDOAR Address
Komplek Golden Plaza Blok G39 - G42 Jl. RS Fatmawati No. 15
Registration Date
Jan 30, 2022
Expiry Date
Jan 31, 2025
Product Type
Therapeutic Gastroenterology-Urology Equipment
Gastrointestinal tube and accessories.
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