BARDEX 3 Way Hematuria Foley Catheter - Indonesia BPOM Medical Device Registration
BARDEX 3 Way Hematuria Foley Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805806073. The device is manufactured by C.R BARD INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SCINTILLATING ASIAN CENTER.
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
Manufacturer
C.R BARD INC.Country of Origin
United States
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
May 20, 2022
Expiry Date
Sep 30, 2025
Product Type
Therapeutic Gastroenterology-Urology Equipment
Urological catheter and accessories.
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