GOODTEC Angiographic Diagnostic Catheter - Indonesia BPOM Medical Device Registration
GOODTEC Angiographic Diagnostic Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501520038. The device is manufactured by GOODMAN CO., LTD. GOODMAN SEKI FACILITY from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAKO TWO MEDICAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GOODMAN CO., LTD. GOODMAN SEKI FACILITYCountry of Origin
Japan
Authorized Representative
PT. MAKO TWO MEDICALAR Address
Rukan Avenue 8 No. 125 dan 127 lantai 1, Jakarta Garden City, Kel. Cakung Timur, Kec. Cakung, Kota Jakarta Timur, Provinsi DKI Jakarta, Kode Pos: 13910
Registration Date
Jan 23, 2025
Expiry Date
Sep 30, 2029
Product Type
Diagnostic Cardiology Equipment
Diagnostic intravascular catheter.
Non Electromedic Sterile

