GEISTLICH Bio-Oss - Indonesia BPOM Medical Device Registration

GEISTLICH Bio-Oss is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602413059. The device is manufactured by GEISTLICH PHARMA AG from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FONDACO JAYATAMA.

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BPOM Registered

Risk Class Kelas Resiko : C

GEISTLICH Bio-Oss

Analysis ID: AKL 20602413059

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

GEISTLICH PHARMA AG

Country of Origin

Switzerland

Authorized Representative

PT. FONDACO JAYATAMA

AR Address

Agung Podomoro Land Tower, Podomoro City Lt. 27 T1, T2, T5 Jl. Letnan Jendral Siswondo Parman Kav. 28 Kel. Tanjung Duren Selatan, Kec. Grogol Petamburan, Jakarta Barat, DKI Jakarta