Neuron 6f 070 Delivery Catheter

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Neuron® Intracranial Access System Penumbra Inc

    https://www.penumbrainc.com/neuro-device/neuron-system/
    Neuron 070. Built with hybrid coil design that allows for dual device delivery via .070″ (1.78 mm) lumen; Full radiopaque platinum distal shaft; Compatible with Penumbra 5 F (1.65 mm) Select Catheters for Rapid Primary Access delivery to final position, eliminating an over-the-wire exchange; Neuron 053.053″ (1.35 mm) lumen for primary ...

Neuron 6F 070 Delivery Catheter* Healthcare Packaging

    https://www.healthcarepackaging.com/issues/regulatory/press-release/13281543/neuron-6f-070-delivery-catheter
    Neuron 6F 070 Delivery Catheter* Penumbra and FDA notified healthcare professionals about a voluntary field removal of the original version of Neuron 6F 070 Delivery Catheter due to reports that the catheter could kink or ovalize in certain anatomical situations, lead to difficulty in catheter advancement and/or delivery of other devices through the guide catheter.

Neuron 6F 070 Delivery Catheter - Parker Waichman LLP

    https://www.yourlawyer.com/defective-medical-devices/recalls/penumbra-recalls-neuron-catheter/
    Oct 01, 2009 · Original Version of Penumbra.Penumbra is initiating a voluntary Field Removal of the original version of its Neuron 6F 070 Delivery Catheter, the U.S. Food and Drug Administration (FDA) just announced. Penumbra has received feedback from some users that these recalled catheters could kink or ovalize in certain anatomical situations.. This kinking and/or ovalization of the catheter lumen …

Penumbra Catheter Recall Issued for Neuron 6F 070 Delivery ...

    https://www.aboutlawsuits.com/penumbra-catheters-recall-neuron-6f-070-delivery-catheter-6238/
    Oct 02, 2009 · Older versions of Penumbra Inc.’s Neuron 6F 070 Delivery Catheter have been recalled in the wake of reports that some catheters have kinked, ovalized or …

MAUDE Adverse Event Report: PENUMBRA, INC. NEURON 6F 070 ...

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=4923400
    The patient was undergoing a medical procedure using a neuron 6f 070 delivery catheter. Upon removal from the packaging, the neuron catheter was found ovalized and was not used. Search Alerts/Recalls : New Search Submit an Adverse Event Report: Brand Name: NEURON 6F 070 DELIVERY CATHETER: Type of Device: DQY: Manufacturer ...

Penumbra Neuron 6F 070 Catheter Recall

    https://www.fda-recalls.us/fda_recall_blog/view/951/penumbra_neuron_6f_070_catheter_recall
    Sep 22, 2009 · The Neuron 6F 070 Delivery Catheter is a component of the Neuron Intracranial Access System, which is used by physicians to introduce medical devices into blood vessels. Recalling Firm: Penumbra, Inc.

Penumbra, PND6F0701058M, 6F, Penumbra Neuron 6F 070 Lumen ...

    https://www.esutures.com/product/1-expired/141-penumbra/1130-guiding-catheters/46262074-penumbra-neuron-6f-070-lumen-delivery-catheter-1058cm-mp-PND6F0701058M/
    Neuron 6F 070 Lumen Delivery Catheter Specifications. Outer Diameter Proximal: 6F; Outer Diameter Distal: 6F; Inner Diameter: 0.070" Wire Compatibility: 0.035" / 0.038" Features. Hybrid shaft design with multi-layer stainless steel braid re-enforced proximal support zone transitioning to …

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