DALLAS Sphygmomanometer - Indonesia BPOM Medical Device Registration
DALLAS Sphygmomanometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501125314. The device is manufactured by GIMA, S.P.A from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDICAL BLESSINGS OF THE ARCHIPELAGO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GIMA, S.P.ACountry of Origin
Italy
Authorized Representative
PT. MEDICAL BLESSINGS OF THE ARCHIPELAGOAR Address
JALAN RUKAN SEDAYU SQUARE BLOK K-19, CENGKARENG
Registration Date
Aug 30, 2021
Expiry Date
Dec 31, 2023
Product Type
Diagnostic Cardiology Equipment
Noninvasive blood pressure measurement system.
Non Electromedic Non Sterile
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