AGFA Hardcopy Imager System Drystar 5302 - Indonesia BPOM Medical Device Registration
AGFA Hardcopy Imager System Drystar 5302 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501811861. The device is manufactured by AGFA ( WUXI ) IMAGING CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GEVAERT AGFA HEALTHCARE INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AGFA ( WUXI ) IMAGING CO., LTD.Country of Origin
China
Authorized Representative
GEVAERT AGFA HEALTHCARE INDONESIAAR Address
Jl. Kesehatan Raya No. 23 C RT 010 RW 011
Registration Date
Oct 27, 2023
Expiry Date
Dec 31, 2027
Product Type
Diagnostic Radiology Equipment
Medical image digitizer.
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