60 results · 78ms · Sources: EU EUDAMED, US FDA

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ONE PART SELDINGER NEEDLE WITHOUT BASEPLATE WITH

FDA Adverse Event
Other ·PROCEDURE PRODUCTS, INC.·Product code DRE·June 17, 2012

DEROYAL

FDA Adverse Event
Other ·DEROYAL INDUSTRIES, INC.·Product code DTL·July 19, 2012

QUILL KNOTLESS ISSUE CLOSUR DEVICE

FDA Adverse Event
Other ·SURGICAL SPECIALITIES PUERTO RICO INC. DBA ANGIOTECH·Product code NEW·July 3, 2013

REPOSABLE STEP

FDA Adverse Event
Other ·INNERDYNE, INC.·Product code DYB·March 10, 1999

STEP

FDA Adverse Event
Other ·INNERDYNE, INC.·Product code GCJ·October 27, 1998

BARD CATHETER STYLET

FDA Adverse Event
Other ·BARD UROLOGICAL PRODUCTS·Product code EZB·August 9, 2006

1721520-1999-00010

FDA Adverse Event
Other ·December 28, 1999

CARRIAZO-BARRAQUER (CB) BLADES

FDA Adverse Event
Other ·MORIA, SA·Product code HMY·October 14, 2002

QUILL KNOTLESS TISSUE CLOSURE DEVICE

FDA Adverse Event
Other ·SURGICAL SPECIALTIES PUERTO RICO INC. DBA ANGIOTECH·Product code NEW·August 29, 2012

SHAMPAINE

FDA Adverse Event
Other ·MAQUET, INC.·Product code FQO·January 27, 2010

C60/5-2 MHZ TRANSDUCER

FDA Adverse Event
Other ·FUJIFILM SONOSITE, INC.·Product code IYN·November 12, 2012

WALGREEN'S 2TSP MEDICINE SPOON

FDA Adverse Event
Other ·APOTHECARY PRODUCTS, INC.·Product code KYX·November 7, 2012

4.5 MM TWIST DRILL

FDA Adverse Event
Other ·AUSTRALIA PTY LTD KNEE DEVELOPMENTS·Product code HTW·July 25, 1997

MAQUET

FDA Adverse Event
Other ·MAQUET S.A.·Product code FSY·March 20, 2009

KARL STORZ

FDA Adverse Event
Other ·KARL STORZ GMBH & CO. KG·Product code KNS·September 13, 2006

MAQUET

FDA Adverse Event
Other ·MAQUET SUZHOU COMPANY LTD·Product code BYX·March 10, 2010

SURGICAL BLADE WITHIN CUSTOM PACK

FDA Adverse Event
Other ·ASPEN SURGICAL PRODUCTS, INC.·Product code GES·June 15, 2012

QUILL KNOTLESS TISSUE CLOSURE DEVICE

FDA Adverse Event
Other ·ANGIOTECH PUERTO RICO INC.·Product code NEW·June 20, 2012

ECHOBED

FDA Adverse Event
Other ·MEDICAL POSITIONING, INC.·Product code LGX·December 26, 2012

PUNCTURE GUARD

FDA Adverse Event
Other ·ICU MEDICAL INC.·Product code FPA·December 13, 2004