BARDEX All Silicone Foley Catheter - Indonesia BPOM Medical Device Registration
BARDEX All Silicone Foley Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805806074. The device is manufactured by HEALTHCARE PRODUCTS from Mexico, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SCINTILLATING ASIAN CENTER.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HEALTHCARE PRODUCTSCountry of Origin
Mexico
Authorized Representative
PT. SCINTILLATING ASIAN CENTERAR Address
JL. Pantai Indah Barat, Komplek TOHO Pantai Indah Kapuk Blok H 25 & 27, Kamal Muara - Penjaringan Jakarta Utara
Registration Date
Mar 13, 2021
Expiry Date
Sep 30, 2025
Product Type
Therapeutic Gastroenterology-Urology Equipment
Urological catheter and accessories.
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