410 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RAUMEDIC-PTO-MONITORING-SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
Phlips Home Nebulizer
FDA UDI
VEGA TECHNOLOGIES INC.·06946159503013·1130529
LEONE SPA
FDA UDI
LEONE SPA·08033707010777·CALIBRA 1ST MOLAR BANDS n.UL 29
MAYO-HEGAR NEEDLE HOLDER
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896021808·MAYO-HEGAR NEEDLE HOLDER SERRATED JAW
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450699119·
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197047166·TC Adson-Brown Forceps
7x7 te...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197047159·TC Adson-Brown Forceps
7x7 te...
LEGEND (BRAND) NITRILE POWDER-FREE PATIENT EXAMINATION GLOVE
FDA 510(k)
FDA Class 1
·General Hospital
LIAISON XL ANALYZER MODEL 10050
FDA 510(k)
FDA Class 2
·Microbiology
ADVANTA 2 BED
FDA Adverse Event
Malfunction
·HILL-ROM DE MEXICO S DE RL DE CV·Product code FNL·March 8, 2013
PRECISION LINK
FDA Adverse Event
Malfunction
·Product code NBW·September 30, 2014
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·June 14, 2011
CAPIOX®FX
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·February 19, 2026
CAPIOX FX25 OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·June 9, 2022
CAPIOX®FX
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·March 30, 2026
CAPIOX FX25 OXYGENATOR
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 6, 2025
CAPIOX FX OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·August 25, 2021
CAPIOX FX25 OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 18, 2022
CAPIOX FX OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 11, 2020
CAPIOX FX OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·September 9, 2024