AXI CATH Female Catheter - Indonesia BPOM Medical Device Registration
AXI CATH Female Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805813228. The device is manufactured by JIANGSU WEIKANG JIEJING MEDICAL APPARATUS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BIO AXION HEALTHINDO.
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.
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
Mar 25, 2021
Expiry Date
Dec 19, 2023
Product Type
Therapeutic Gastroenterology-Urology Equipment
Urological catheter and accessories.
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