E-LUMINEXX Vascular Stent - Indonesia BPOM Medical Device Registration
E-LUMINEXX Vascular Stent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003125138. 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
MT Haryono Square Lantai 1 Unit 1, Jl. Otto Iskandardinata Raya No. 390 RT 006 RW 012 Kel. Bidara Cina, Kec. Jatinegara, Jakarta Timur, DKI Jakarta
Registration Date
Aug 23, 2021
Expiry Date
Sep 24, 2025
Product Type
Therapeutic Neurology Equipment
Peripheral Stent
Non Electromedic Sterile
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