FemoStop ™ II Plus System Set - Indonesia BPOM Medical Device Registration
FemoStop ™ II Plus System Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504027588. The device is manufactured by ST JUDE MEDICAL PUERTO RICO., LLC from Puerto Rico USA, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ST JUDE MEDICAL PUERTO RICO., LLCCountry of Origin
Puerto Rico USA
Authorized Representative
PT. TAWADA HEALTHCAREAR Address
Rukan Permata Senayan Blok A18-19 Lantai 1-2 Jl. Tentara Pelajar No. 5
Registration Date
Dec 07, 2020
Expiry Date
Aug 01, 2024
Product Type
Surgical Cardiology Equipment
Vascular clamp.
Non Electromedic Sterile
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