14 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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QUIKCLOT INTEVENTIONAL, MODEL P/N 182
FDA 510(k)
FDA Unclassified
·Unknown
Symmetry Surgical®
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482144305·Probe, Double-Ended, Silver, 8 in
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450208779·
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962108796·PROBE, 8", DOUBLE ENDED, SLIVER
ENDOSCOPIC STAPLE REMOVAL INSTRUMENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PBN FALLOPIAN TUBE CATHETER SYSTEM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FSA·May 2, 2013
LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code LDD·September 15, 2014
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 26, 2011
BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code PJE·February 8, 2023
ONYX
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·October 2, 2024
REBAR
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·October 2, 2024
BD SYRINGE 3ML HEPARIN
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NZW·September 9, 2019
Copeland HA Resurfacing Head, MB/HA EAS Head; Item Nos. 11-114641 11-114642 11-114643 11-114644 11-114644S 11-114645 11-114646 11-114647 11-114648 11-114661 11-114662 11-114663 11-114664 11-114664S 11-114665 11-114666 11-114667 11-114668 11-114632 11-114633 Product Usage: Partial Shoulder Replacement.
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·December 4, 2019