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 20502614031. The device is manufactured by DIXION SALES OF MEDICAL DEVICES 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 SALES OF MEDICAL DEVICES GMBH.Country of Origin
Germany
Authorized Representative
PT. MEDIKA INDO BAVARIAAR Address
Ruko Green Garden Blok A 14 No. 10 RT. 05 / RW. 03
Registration Date
Dec 04, 2021
Expiry Date
Sep 10, 2026
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
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