BOSCH Vivatmo me Asia - Indonesia BPOM Medical Device Registration
BOSCH Vivatmo me Asia is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103220226. The device is manufactured by BOSCH HEALTHCARE SOLUTIONS GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MRK DIAGNOSTICS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BOSCH HEALTHCARE SOLUTIONS GMBHCountry of Origin
Germany
Authorized Representative
MRK DIAGNOSTICSAR Address
JL. Merpati Mas I Blok B1 NO.46 Perkantoran Tanjung Mas Raya Tanjung Barat
Registration Date
Dec 26, 2022
Expiry Date
Oct 13, 2027
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