Kii Balloon Blunt Tip System - Indonesia BPOM Medical Device Registration
Kii Balloon Blunt Tip System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801420409. The device is manufactured by APPLIED MEDICAL RESOURCES CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
APPLIED MEDICAL RESOURCES CORPORATIONCountry of Origin
United States
Authorized Representative
BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
Nov 21, 2024
Expiry Date
Dec 31, 2026
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories.
Non Electromedic Sterile
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