AGFA E.O.S Developer - Indonesia BPOM Medical Device Registration
AGFA E.O.S Developer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11501812579. The device is manufactured by AGFA N.V. from Belgium, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GEVAERT AGFA HEALTHCARE INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
AGFA N.V.Country of Origin
Belgium
Authorized Representative
PT. GEVAERT AGFA HEALTHCARE INDONESIAAR Address
Jl. Kesehatan Raya No. 23 C RT 010 RW 011
Registration Date
Apr 18, 2023
Expiry Date
Apr 05, 2027
Product Type
Diagnostic Radiology Equipment
Radiographic film.
Non Electromedic Non Sterile
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