NIHON KOHDEN Elefix Paste for EEG - Indonesia BPOM Medical Device Registration
NIHON KOHDEN Elefix Paste for EEG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21001025021. The device is manufactured by NIHON KOHDEN TOMIOKA CORPORATION TOMIOKA PRODUCTION CENTER. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PETAN DAYA MEDICA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Japan
Authorized Representative
PETAN DAYA MEDICAAR Address
Komplek Setia Budi Point Jl. Setia Budi Blok C No. 3-4 Medan
Registration Date
Mar 30, 2023
Expiry Date
Mar 31, 2026
Product Type
Diagnostic Neurology Equipment
Electroencephalograph.
Non Electromedic Non Sterile
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