TURNPIKE LP Catheter - Indonesia BPOM Medical Device Registration
TURNPIKE LP Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505420055. The device is manufactured by VASCULAR SOLUTIONS LLC from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. TELEFLEX MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
VASCULAR SOLUTIONS LLCCountry of Origin
United States
Authorized Representative
PT. TELEFLEX MEDICAL INDONESIAAR Address
Wisma 46 - Kota BNI Lantai 47, Units 01-04, Jl. Jend. Sudirman Kav. 1
Registration Date
Apr 24, 2024
Expiry Date
Nov 14, 2028
Product Type
Therapeutic Cardiology Equipment
Percutaneous catheter for coronary use
Non Electromedic Sterile
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