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RPM Reinforced PTFE Mesh - Indonesia BPOM Medical Device Registration

RPM Reinforced PTFE Mesh is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602122028. 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
RPM Reinforced PTFE Mesh
Analysis ID: AKL 20602122028

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 11, 2024

Expiry Date

Aug 22, 2029

Product Type

Prosthetic Dental Equipment

Bone grafting material.

Non Electromedic Sterile

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