ASPEL Electrocardiograph - Indonesia BPOM Medical Device Registration
ASPEL Electrocardiograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501110621. The device is manufactured by ASPEL S.A. from Poland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ALKESTRON SELF-SOURCE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ASPEL S.A.Country of Origin
Poland
Authorized Representative
PT. ALKESTRON SELF-SOURCEAR Address
Komplek Ruko Griya Inti Sentosa, JI. Griya Agung Blok O No.95, RT.2/RW.20
Registration Date
May 02, 2024
Expiry Date
Feb 23, 2029
Product Type
Monitoring Cardiology Equipment
Electrocardiograph.
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