AGFA CR 10-X - Indonesia BPOM Medical Device Registration
AGFA CR 10-X is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501814927. The device is manufactured by AGFA-GEVAERT HEALTHCARE GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GEVAERT AGFA HEALTHCARE INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AGFA-GEVAERT HEALTHCARE GMBH.Country of Origin
Germany
Authorized Representative
PT. GEVAERT AGFA HEALTHCARE INDONESIAAR Address
Jl. Kesehatan Raya No. 23 C RT 010 RW 011
Registration Date
Feb 01, 2021
Expiry Date
Nov 23, 2023
Product Type
Diagnostic Radiology Equipment
Medical image digitizer.
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