DIXION Patient Monitor - Indonesia BPOM Medical Device Registration
DIXION Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502123613. The device is manufactured by DIXION VERTRIEB MEDIZINISCHER GERÄTE GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDIKA INDO BAVARIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIXION VERTRIEB MEDIZINISCHER GERÄTE GMBHCountry of Origin
Germany
Authorized Representative
PT. MEDIKA INDO BAVARIAAR Address
Ruko Green Garden Blok A 14 No. 10 RT. 05 / RW. 03
Registration Date
Feb 20, 2022
Expiry Date
Sep 10, 2026
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
Non Radiation Electromedics
TWINSTREAM
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