FOKUS General Instrument Set I - Indonesia BPOM Medical Device Registration
FOKUS General Instrument Set I is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603918147. The device is manufactured by CEATEC MEDIZINTECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FOCUS DIAGNOSTIC INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CEATEC MEDIZINTECHNIK GMBHCountry of Origin
Germany
Authorized Representative
PT. FOCUS DIAGNOSTIC INDONESIAAR Address
Jl. Jatipadang Raya No.9A, RT.6/RW.4, Kelurahan Jatipadang, Kecamatan Pasar Minggu, Kota Jakarta Selatan, DKI Jakarta 12540
Registration Date
Nov 16, 2022
Expiry Date
Nov 16, 2025
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Non Sterile
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