KII Low Profile Optical Access System - Indonesia BPOM Medical Device Registration
KII Low Profile Optical Access System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801420416. 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 PT. BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
APPLIED MEDICAL RESOURCES CORPORATIONCountry of Origin
United States
Authorized Representative
PT. BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
Nov 25, 2024
Expiry Date
Dec 31, 2026
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories.
Non Electromedic Sterile
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