OSTEOMED 2.0 Orthognatic Instruments - Indonesia BPOM Medical Device Registration
OSTEOMED 2.0 Orthognatic Instruments is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303121783. The device is manufactured by OSTEOMED from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PRO-HEALTH INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
OSTEOMEDCountry of Origin
United States
Authorized Representative
PRO-HEALTH INTERNATIONALAR Address
Komplek Perkantoran Duta Merlin Blok C 35-36 Jalan Gajah Mada 3-5
Registration Date
Dec 08, 2022
Expiry Date
Jul 05, 2027
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Non Sterile
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