SHINOBI Plus Steerable Guidewire - Indonesia BPOM Medical Device Registration
SHINOBI Plus Steerable Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320850. The device is manufactured by LAKE REGION MEDICAL LTD. from Ireland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. WEGO MEDIKA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LAKE REGION MEDICAL LTD.Country of Origin
Ireland
Authorized Representative
PT. WEGO MEDIKA INDONESIAAR Address
Jl. Tanah Abang II No.67 Kel. Petojo Selatan, Kec. Gambir, Jakarta Pusat
Registration Date
Mar 28, 2024
Expiry Date
May 01, 2028
Product Type
Diagnostic Cardiology Equipment
Catheter guide wire.
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