FKG Reamers - Indonesia BPOM Medical Device Registration
FKG Reamers is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603514757. The device is manufactured by FKG DENTAIRE S.A. from Switzerland, 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
FKG DENTAIRE S.A.Country of Origin
Switzerland
Authorized Representative
PT. BINTANG SAUDARA SEMESTA JAYAAR Address
Jl.Asia No.212 A-B, Medan
Registration Date
May 10, 2019
Expiry Date
Feb 19, 2024
Product Type
Surgical Dental Equipment
Dental hand instrument.
Non Electromedic Non Sterile
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