TENSIOMED Arteriograph - Indonesia BPOM Medical Device Registration
TENSIOMED Arteriograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501321080. The device is manufactured by TENSIOMED LTD. from Hungary, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN MEDICAL PARTNERS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TENSIOMED LTD.Country of Origin
Hungary
Authorized Representative
PT. MAIN MEDICAL PARTNERSAR Address
JL. DR. Wahidin No 68 D,
Registration Date
Oct 17, 2023
Expiry Date
Jun 30, 2026
Product Type
Diagnostic Cardiology Equipment
Noninvasive blood pressure measurement system.
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