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CYTOPLAST Ti-250/150 Titanium-Reinforced - Indonesia BPOM Medical Device Registration

CYTOPLAST Ti-250/150 Titanium-Reinforced is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602024937. The device is manufactured by OSTEOGENICS BIOMEDICAL, INC. from United States, 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
CYTOPLAST Ti-250/150 Titanium-Reinforced
Analysis ID: AKL 20602024937

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

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

Registration Date

Oct 07, 2024

Expiry Date

Aug 22, 2029

Product Type

Prosthetic Dental Equipment

Bone grafting material.

Non Electromedic Sterile

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