AGFA Digital Detector with Automatic Exposure Detection (AED) - Indonesia BPOM Medical Device Registration
AGFA Digital Detector with Automatic Exposure Detection (AED) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11501811676. The device is manufactured by VIEWORKS CO., LTD. from Korea, 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
VIEWORKS CO., LTD.Country of Origin
Korea
Authorized Representative
PT. GEVAERT AGFA HEALTHCARE INDONESIAAR Address
Jl. Kesehatan Raya No. 23 C RT 010 RW 011
Registration Date
Dec 19, 2022
Expiry Date
Apr 05, 2027
Product Type
Diagnostic Radiology Equipment
Medical image communications device.
Non Radiation Electromedics
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