AIDUROL Hydrophilic Guidewire - Indonesia BPOM Medical Device Registration
AIDUROL Hydrophilic Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501520034. The device is manufactured by SCW MEDICATH LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ABADI PERKASA WITH ALKESINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SCW MEDICATH LTD.Country of Origin
China
Authorized Representative
PT. ABADI PERKASA WITH ALKESINDOAR Address
Ruko Prominence Blok 38 E Nomor 56, Jalan Jalur Sutera Barat, RT.003/006
Registration Date
Jan 17, 2025
Expiry Date
May 31, 2027
Product Type
Diagnostic Cardiology Equipment
Catheter guide wire.
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