ADSCOPE 605 - Indonesia BPOM Medical Device Registration
ADSCOPE 605 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10501311176. The device is manufactured by AMERICAN DIAGNOSTIC CORPORATION from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GLOBAL SYSTECH MEDIKA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
AMERICAN DIAGNOSTIC CORPORATIONCountry of Origin
United States
Authorized Representative
PT. GLOBAL SYSTECH MEDIKAAR Address
Jl. TB Simatupang No.17 RT.011/002 Kel. Susukan, Kec. Ciracas Jakarta Timur
Registration Date
Feb 07, 2022
Expiry Date
Feb 01, 2027
Product Type
Diagnostic Cardiology Equipment
Stethoscope.
Non Electromedic Non Sterile
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