Glidesheath Slender - Indonesia BPOM Medical Device Registration
Glidesheath Slender is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420392. The device is manufactured by TERUMO VIETNAM CO., LTD. from Vietnam, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TERUMO VIETNAM CO., LTD.Country of Origin
Vietnam
Authorized Representative
TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Jul 29, 2024
Expiry Date
Jan 30, 2029
Product Type
Diagnostic Cardiology Equipment
Catheter introducer.
Non Electromedic Sterile
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