POWERBONE Putty - Indonesia BPOM Medical Device Registration
POWERBONE Putty is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302125739. The device is manufactured by BONEGRAFT BIOLOGICAL MATERIALR SAN. AND. T.C. Inc. from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAGNIFICENT DINAR CALAKAN.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Turkey
Authorized Representative
PT. MAGNIFICENT DINAR CALAKANAR Address
Jl. Danita 2 Kav 2 RT 015 RW 013, Kel. Bekasijaya, Kec. Bekasi Timur, Kota Bekasi, Jawa Barat
Registration Date
Dec 21, 2023
Expiry Date
Dec 01, 2026
Product Type
Prosthetic Orthopedic Equipment
Resorbable calcium salt bone void filler device.
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