MYRA BMS Balloon Expandable Peripheral Stent System - Indonesia BPOM Medical Device Registration
MYRA BMS Balloon Expandable Peripheral Stent System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503611541. The device is manufactured by MERIL LIFE SCIENCES PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MSR GREEN LESTARI.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
MERIL LIFE SCIENCES PVT. LTD.Country of Origin
India
Authorized Representative
PT. MSR GREEN LESTARIAR Address
Jl. Agung Utara I A2 - 27 Sunter Agung Podomoro. Telp : 021-65307518
Registration Date
Mar 23, 2023
Expiry Date
Jan 16, 2026
Product Type
Prosthetic Cardiology Equipment
Coronary stent
Non Electromedic Sterile
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