EUCALIMUS Sirolimus Eluting Stent - Indonesia BPOM Medical Device Registration
EUCALIMUS Sirolimus Eluting Stent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503028107. The device is manufactured by EUCATECH AT from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is DIAN LANGGENG PRATAMA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
EUCATECH ATCountry of Origin
Germany
Authorized Representative
DIAN LANGGENG PRATAMAAR Address
Jl. Raden Saleh Raya No. 4
Registration Date
Jul 18, 2022
Expiry Date
Dec 31, 2024
Product Type
Prosthetic Cardiology Equipment
Drug eluting stent
Non Electromedic Sterile
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