BARD® Polyester Felt - Indonesia BPOM Medical Device Registration
BARD® Polyester Felt is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20503712510. The device is manufactured by BARD SHANNON LIMITED from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PERMATA BUNDA ARTANO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BARD SHANNON LIMITEDCountry of Origin
United States
Authorized Representative
PERMATA BUNDA ARTANOAR Address
Jl. Hos. Cokroaminoto, Komp. Perkantoran CBD Ciledug Blok A3 No. 17, Ciledug 15157
Registration Date
Oct 22, 2020
Expiry Date
Dec 31, 2023
Product Type
Prosthetic Cardiology Equipment
Intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or polytetrafluoroethylene.
Non Electromedic Sterile
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BARD® Edwards Outflow Tract Fabric
BARD® Polyester Cardiovascular Fabrics
BARD® PTFE Braided Tape
BARD® Polyester Braided Tape
FEHLING INSTRUMENTS Rodents I
FEHLING INSTRUMENTS GMBH & CO. KG.
FEHLING INSTRUMENTS Rodents II
FEHLING INSTRUMENTS GMBH & CO. KG.
FEHLING INSTRUMENTS Container
FEHLING INSTRUMENTS GMBH & CO. KG
FEHLING INSTRUMENTS Retractors II
FEHLING INSTRUMENTS GMBH & CO. KG.
FEHLING INSTRUMENTS Clamps I
FEHLING INSTRUMENTS GMBH & CO. KG.
FEHLING INSTRUMENTS Cannulae
FEHLING INSTRUMENTS GMBH & CO. KG.
IMPRA Carboflo ePTFE Vascular Grafts
BARD PERIPHERAL VASCULAR, INC.
BARD® Polyester Braided Tape
BARD SHANNON LIMITED
DYNAFLO® Bypass Grafts
BARD PERIPHERAL VASCULAR, INC.

