OSTEOMED 2.0 Orthogantic System - Indonesia BPOM Medical Device Registration
OSTEOMED 2.0 Orthogantic System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603213140. The device is manufactured by OSTEOMED from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PRO-HEALTH INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
OSTEOMEDCountry of Origin
United States
Authorized Representative
PT. PRO-HEALTH INTERNATIONALAR Address
Komplek Perkantoran Duta Merlin Blok C 35-36 Jalan Gajah Mada 3-5
Registration Date
Dec 06, 2022
Expiry Date
Jul 05, 2027
Product Type
Surgical Dental Equipment
Bone plate.
Non Electromedic Non Sterile
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