KINETEC Shoulder CPM Machine - Indonesia BPOM Medical Device Registration
KINETEC Shoulder CPM Machine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403911577. The device is manufactured by KINETEC SAS from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is GLOBAL SYSTECH MEDIKA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
KINETEC SASCountry of Origin
France
Authorized Representative
GLOBAL SYSTECH MEDIKAAR Address
Jl. TB Simatupang No.17 RT.011/002 Kel. Susukan, Kec. Ciracas Jakarta Timur
Registration Date
Jul 17, 2023
Expiry Date
May 19, 2028
Product Type
Therapeutic Physical Health Equipment
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