IMPRA® ePTFE Vascular Grafts - Indonesia BPOM Medical Device Registration
IMPRA® ePTFE Vascular Grafts is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20503712515. The device is manufactured by BARD PERIPHERAL VASCULAR, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GEM OF MOTHER ARTANO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BARD PERIPHERAL VASCULAR, INC.Country of Origin
United States
Authorized Representative
PT. GEM OF MOTHER ARTANOAR Address
Jl. Hos. Cokroaminoto, Komp. Perkantoran CBD Ciledug Blok A3 No. 17, Ciledug 15157
Registration Date
Mar 17, 2021
Expiry Date
Dec 31, 2023
Product Type
Prosthetic Cardiology Equipment
Vascular graft prosthesis.
Non Electromedic Sterile
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FEHLING INSTRUMENTS Retractors III
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FEHLING INSTRUMENTS Holding and Guiding Instruments
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FEHLING INSTRUMENTS Aortic Punches
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FEHLING INSTRUMENTS Gauges and Sizing Instruments
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FEHLING INSTRUMENTS Forceps I
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FEHLING INSTRUMENTS Dissectors
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FEHLING INSTRUMENTS Clamps II
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FEHLING INSTRUMENTS Forceps III
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