57 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Paonan Armstrong Posterior Spinal Fixation System
FDA 510(k)
FDA Class 2
·Orthopedic
LoFric® Sense™
FDA UDI
Wellspect AB·07333387022468·Single Use Urinary Catheter with salt solution....
LoFric® Sense™
FDA UDI
Wellspect AB·07392532086281·Single Use Urinary Catheter with salt solution....
Vilex Power Accessory
FDA UDI
VILEX IN TENNESSEE, INC.·00841731122285·KWire .062x9" (1.6x225mm)
Vilex Power Accessory
FDA UDI
VILEX IN TENNESSEE, INC.·00841731122230·KWire .045x9" (1.1x225mm)
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321612250·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311612250·
STRYKER DISPOSABLE LAPAROSCOPIC SCISSORS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PROMIMIC DENTAL IMPLANT, 3.75 MM, LENGTH 8.5 MM MODEL 03-1001, PROMIMIC DENTAL IMPLANT, 3.75 MM, LENGTH 10 MM MODEL 03-1
FDA 510(k)
FDA Class 2
·Dental
NI
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·August 29, 2016
NI
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·August 24, 2016
NI
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FPA·October 3, 2016
ICY
FDA Adverse Event
ZOLL MEDICAL CORPORATION·Product code NCX·July 6, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013
COLLEAGUE 3 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 17, 2008
CLEARLINK DUO-VENT CONTINU-FLO SOLUTION SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·October 1, 2020
CLEARLINK CONTINU-FLO SOLUTION SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·December 6, 2021
CLEARLINK DUO-VENT CONTINU-FLO SOLUTION SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·August 14, 2020
CLEARLINK CONTINU-FLO SOLUTION SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·November 8, 2021
HF UNIT "ESG-400"
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GEI·April 23, 2021