ACTIVE X-RAY Film Viewer - Indonesia BPOM Medical Device Registration
ACTIVE X-RAY Film Viewer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11501027340. The device is manufactured by AKTIF DIS TIC. ÝNŞ. TURZ. VE TIBBI URUN SAN. LTD. STI. from Turkey, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is TRI MEDITAMA BRILLIANTLY.
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AKTIF X-RAY Film Viewer
Risk Classification
Product Class
Kelas : 1
Country of Origin
Turkey
Authorized Representative
TRI MEDITAMA BRILLIANTLYAR Address
Ruko Sentra Primer Timur Commercial Park 1 No. 03, Jl. Sentra Premier Timur
Registration Date
Nov 29, 2020
Expiry Date
Jun 18, 2025
Product Type
Diagnostic Radiology Equipment
Radiographic film illuminator.
Non Radiation Electromedics
