THOMAS INSTRUMENTS - Indonesia BPOM Medical Device Registration
THOMAS INSTRUMENTS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10602320580. The device is manufactured by FFDM TIVOLY from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MANDALA MITRATAMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
FFDM TIVOLYCountry of Origin
France
Authorized Representative
MANDALA MITRATAMAAR Address
Komplek Ruko Roxy Mas Blok C 2 No. 12 Jl. Hasyim Ashari 125
Registration Date
May 16, 2023
Expiry Date
Nov 30, 2027
Product Type
Prosthetic Dental Equipment
Root canal post.
Non Electromedic Non Sterile
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