BARD E-LUMINEXX Biliary Stent - Indonesia BPOM Medical Device Registration
BARD E-LUMINEXX Biliary Stent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805121256. The device is manufactured by ANGIOMED GMBH & CO. MEDIZINTECHNIK KG from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ITAMA RANORAYA.
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Risk Classification
Product Class
Kelas : 2
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
Mar 09, 2021
Expiry Date
Sep 24, 2025
Product Type
Therapeutic Gastroenterology-Urology Equipment
Biliary catheter and accessories.
Non Electromedic Sterile
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