MEDG All Silicone Foley Catheter 3way - Indonesia BPOM Medical Device Registration
MEDG All Silicone Foley Catheter 3way is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320975. The device is manufactured by JIANGSU PROVINCE HUAXING MEDICAL APPARATUS INDUSTRY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ALEXA MEDIKA.
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. ALEXA MEDIKAAR Address
Jl. Yos Sudarso Komplek Graha Niaga Blok C No. 14
Registration Date
Oct 22, 2023
Expiry Date
Mar 10, 2028
Product Type
Therapeutic Gastroenterology-Urology Equipment
Urological catheter and accessories.
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