PRIMAMED DUODYNATOR - Indonesia BPOM Medical Device Registration
PRIMAMED DUODYNATOR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403211062. The device is manufactured by GBO MEDIZINTECHNIK AG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DAYA PRIMA MANDIRI JAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GBO MEDIZINTECHNIK AG.Country of Origin
Germany
Authorized Representative
PT. DAYA PRIMA MANDIRI JAYAAR Address
JL. KALIGARANG 1A SEMARANG
Registration Date
Aug 01, 2019
Expiry Date
Feb 18, 2024
Product Type
Therapeutic Physical Health Equipment
Powered muscle stimulator.
Non Radiation Electromedics
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