DIO Abutment - Indonesia BPOM Medical Device Registration
DIO Abutment is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602022141. The device is manufactured by DIO CORPORATION from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BINTANG SAUDARA SEMESTA JAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIO CORPORATIONCountry of Origin
Korea
Authorized Representative
PT. BINTANG SAUDARA SEMESTA JAYAAR Address
Jl.Asia No.212 A-B, Medan
Registration Date
May 28, 2020
Expiry Date
Jul 29, 2024
Product Type
Prosthetic Dental Equipment
Endosseous dental implant abutment.
Non Electromedic Non Sterile
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