40 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PALS NEONATAL PEDIATRIC ECG ELECTRODE, MODELS PN100, PN200
FDA 510(k)
FDA Class 2
·Cardiovascular
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950016563·CURETTE BONE MILLER #12 D/E 7" 18CM TIP SIZE AP...
intellijoint HIP®
FDA UDI
Intellijoint Surgical Inc·00628184002063·V-Block, G2
SCHWERT
FDA UDI
A. Schweickhardt GmbH & Co. KG·E89620002060·Needle holders 18cm curved diamond
coated...
SILVERVENT
FDA UDI
Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948000214·SILVERVENT 2 IC, SIZE 6
PRCT2
FDA UDI
FX SOLUTIONS·03701037301869·PRCT2, DIAPHYSEAL PLATE TA6V 6 HOLES
Matrix Wearable
FDA UDI
GLOBAL INSTRUMENTATION, LLC·00815187020112·M5 Patient Cable Cradle
BONE SCREWS DIA. 6.5 X H. 35 MM
FDA Adverse Event
Malfunction
·LIMACORPORATE SPA·Product code LPH·March 24, 2022
FlowLogic Agile
FDA UDI
SONENDO, INC.·00810209420161·FlowLogic Agile Shaping File 20/.06, 21mm
IMMULITE PHENYTOIN, IMMULITE 2000 PHENYTOIN, CATALOG # LKPN1, LKPN5 & L2KPN2, L2KPN6
FDA 510(k)
FDA Class 2
·Clinical Toxicology
APPLE MEDICAL ONE-TOUCH UTERINE SAMPLER
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
FEMORAL MODULAR HEAD - L Ø36MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code LPH·August 9, 2022
CARDIOSAVE HYBRID W/ E/F PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·January 15, 2025
5.0CM SHORT ATTACHMENT
FDA Adverse Event
Malfunction
·THE ANSPACH EFFORT, INC.·Product code HBC·February 14, 2013
SELOX ST 60
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code NVZ·February 18, 2011
DISPOSABLE PURSTRING 65 INSTRUMENT
FDA Adverse Event
Injury
·PONCE - USS·Product code GAG·February 19, 2008
3MM ELASTIC STAYS 8/PK
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code GAD·September 27, 2024
AIA-900
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·January 28, 2019
SMR CEMENTLESS FINNED STEM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code HSD·March 11, 2022
Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A, View Station Software Kit 0020-00-0206-16A, Work Station Software Kit 0020-00-0207-16A, Software Kit Upgrade TECH-00-910. The Panaroma Patient Monitoring Network is intended for use in a fixed location in the healthcare facility setting as a central viewing station. It is not intended to be directly connected to patient at any time or installed in a patient's vicinity.
FDA Recall
Terminated
·Mindray DS USA, Inc. dba Mindray North America·Product code MHX·December 15, 2015