Teleflex Incorporated TFX recently received the FDA’s 510(k) clearance to expand the Indications for Use of its Arrow EZ-IO Intraosseous (IO) Vascular Access System. With the expanded indication, the ...
Teleflex Corporation TFX recently announced that the FDA has granted 510(k) clearance to e Arrow EZ-IO Needle — the first and only intraosseous (IO) needle — for MR Conditional labeling. The ...
WAYNE, Pa., June 06, 2023 (GLOBE NEWSWIRE) -- Teleflex Incorporated (TFX), a leading global provider of medical devices for critical care and surgery, today announced that the Arrow ® EZ-IO ® Needle ...
WAYNE, Pa., Oct. 01, 2020 (GLOBE NEWSWIRE) -- Teleflex Incorporated (NYSE: TFX), a leading global provider of medical devices for critical care and surgery, has announced it has received 510(k) ...
Teleflex Incorporated TFX recently received the FDA’s 510(k) clearance to expand the Indications for Use of its Arrow EZ-IO Intraosseous (IO) Vascular Access System. With the expanded indication, the ...
Teleflex Incorporated TFX recently received the FDA’s 510(k) clearance to expand the Indications for Use of its Arrow EZ-IO Intraosseous (IO) Vascular Access System. With the expanded indication, the ...
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