DEYMED SomniPro PSG CL System - Indonesia BPOM Medical Device Registration
DEYMED SomniPro PSG CL System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21001420040. The device is manufactured by DEYMED DIAGNOSTIC S.R.O from Czech Republic, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN MEDICAL PARTNERS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DEYMED DIAGNOSTIC S.R.OCountry of Origin
Czech Republic
Authorized Representative
PT. MAIN MEDICAL PARTNERSAR Address
JL. DR. Wahidin No 68 D,
Registration Date
Oct 02, 2024
Expiry Date
Dec 31, 2026
Product Type
Diagnostic Neurology Equipment
Electroencephalograph.
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