DIO Surgical Tool - Indonesia BPOM Medical Device Registration
DIO Surgical Tool is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603022119. The device is manufactured by DIO CORPORATION from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BINTANG SAUDARA SEMESTA JAYA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
DIO CORPORATIONCountry of Origin
Korea
Authorized Representative
PT. BINTANG SAUDARA SEMESTA JAYAAR Address
Jl.Asia No.212 A-B, Medan
Registration Date
Apr 19, 2020
Expiry Date
Jul 30, 2024
Product Type
Surgical Dental Equipment
Dental hand instrument
Non Electromedic Non Sterile
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