KONICA MINOLTA Medical Imaging Film SD-S - Indonesia BPOM Medical Device Registration
KONICA MINOLTA Medical Imaging Film SD-S is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11501220104. The device is manufactured by CARESTREAM HEALTH, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MURSMEDIC.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CARESTREAM HEALTH, INC.Country of Origin
United States
Authorized Representative
MURSMEDICAR Address
Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat
Registration Date
Jun 05, 2023
Expiry Date
Jul 14, 2025
Product Type
Diagnostic Radiology Equipment
Radiographic film.
Non Electromedic Non Sterile
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