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., 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) ...
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 ...
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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