LIFESTENT Vascular Stent - Indonesia BPOM Medical Device Registration
LIFESTENT Vascular Stent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503121751. The device is manufactured by ANGIOMED GMBH & CO. MEDIZINTECHNIK KG from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ITAMA RANORAYA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
ANGIOMED GMBH & CO. MEDIZINTECHNIK KGCountry of Origin
Germany
Authorized Representative
PT. ITAMA RANORAYAAR Address
JL. OTTO ISKANDARDINATA RAYA NO. 390, GEDUNG MT. HARYONO SQUARE LANTAI 1 UNIT 1, Desa/Kelurahan Bidara Cina, Kec. Jatinegara, Kota Adm. Jakarta Timur, Provinsi DKI Jakarta, Kode Pos: 13330
Registration Date
Aug 18, 2023
Expiry Date
Sep 24, 2025
Product Type
Prosthetic Cardiology Equipment
Superficial Femoral Artery Stent
Non Electromedic Sterile
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