BISCO All-Bond Universal - Indonesia BPOM Medical Device Registration
BISCO All-Bond Universal is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602811199. The device is manufactured by BISCO, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FONDACO JAYATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BISCO, INC.Country of Origin
United States
Authorized Representative
PT. FONDACO JAYATAMAAR 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
Mar 01, 2022
Expiry Date
Dec 15, 2025
Product Type
Prosthetic Dental Equipment
Resin tooth bonding agent.
Non Electromedic Non Sterile
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