M-CATH FLEXY Microcatheter - Indonesia BPOM Medical Device Registration
M-CATH FLEXY Microcatheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501220236. The device is manufactured by ACROSTAK (SCHWEIZ) AG. from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is HARMONY PRIMA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ACROSTAK (SCHWEIZ) AG.Country of Origin
Switzerland
Authorized Representative
HARMONY PRIMA MEDIKAAR Address
Jl. Tanjung Selor No. 1A, Cideng, Gambir, Jakarta Pusat, 10150
Registration Date
Jun 23, 2022
Expiry Date
Aug 26, 2026
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
Non Electromedic Sterile
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