PUROFLEX Uretheral Stent Set - Indonesia BPOM Medical Device Registration
PUROFLEX Uretheral Stent Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805806873. 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. SCINTILLATING ASIAN CENTER.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ANGIOMED GMBH & CO. MEDIZINTECHNIK KGCountry of Origin
Germany
Authorized Representative
PT. SCINTILLATING ASIAN CENTERAR Address
JL. Pantai Indah Barat, Komplek TOHO Pantai Indah Kapuk Blok H 25 & 27, Kamal Muara - Penjaringan Jakarta Utara
Registration Date
Dec 03, 2020
Expiry Date
Aug 20, 2025
Product Type
Gastroenterology-Surgical Urology Equipment
Ureteral stent.
Non Electromedic Sterile
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