BEURER Pulse Oximeter - Indonesia BPOM Medical Device Registration
BEURER Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502026503. The device is manufactured by BEURER GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SERENITY INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BEURER GMBH.Country of Origin
Germany
Authorized Representative
SERENITY INDONESIAAR Address
Komplek Ruko Permata Kota Blok Q No. 10 Jl. Pangeran Tubagus Angke No.170 RT.010 RW . 01
Registration Date
Jun 16, 2023
Expiry Date
Mar 31, 2026
Product Type
Monitoring Cardiology Equipment
Oximeter.
Non Radiation Electromedics
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