26 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OPTIPORE SCRUB SPONGE
FDA 510(k)
FDA Unclassified
·Unknown
Spex Limited
FDA UDI
SPEX LIMITED·09420051709898·Power Recline Adapter Mount
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K1102000·Tray, 2 inch base
N/A
FDA UDI
Stryker Leibinger GmbH & Co. KG·07613327638196·Spine Guidance 5 Update
UniTip Catheter
FDA UDI
Unisensor AG·07640172972083·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971581·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971598·
UniTip Catheter
FDA UDI
Unisensor AG·07640172972076·
1 ml Sterile Hypodermic Syringe For Single Use. With/Without Needle. Luer/Luer-Lock
FDA 510(k)
FDA Class 2
·General Hospital
ESG-300, APU-300, Pressure Reducer, MAPC Probes
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DEROYAL
FDA Adverse Event
Malfunction
·DEROYAL GUATEMALA·Product code FMQ·February 5, 2014
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 24, 2007
VAPOTHERM DISPOSABLE PT CIRCUIT
FDA Adverse Event
Other
·VAPOTHERM, INC·Product code BTT·October 3, 2012
ELECTROSURGICAL GENERATOR "ESG-300"
FDA Adverse Event
Injury
·OLYMPUS WINTER & IBE GMBH·Product code GEI·September 29, 2021
ELECTROSURGICAL GENERATOR "ESG-300"
FDA Adverse Event
Injury
·OLYMPUS WINTER & IBE GMBH·Product code GEI·March 18, 2020
ELECTROSURGICAL GENERATOR "ESG-300"
FDA Adverse Event
Injury
·OLYMPUS WINTER & IBE GMBH·Product code GEI·September 30, 2020
ELECTROSURGICAL GENERATOR "ESG-300"
FDA Adverse Event
Injury
·OLYMPUS WINTER & IBE GMBH·Product code GEI·October 26, 2021
ELECTROSURGICAL GENERATOR "ESG-300"
FDA Adverse Event
Injury
·OLYMPUS WINTER & IBE GMBH·Product code GEI·July 29, 2022
ELECTROSURGICAL GENERATOR "ESG-300"
FDA Adverse Event
Injury
·OLYMPUS WINTER & IBE GMBH·Product code GEI·January 24, 2020
ELECTROSURGICAL GENERATOR "ESG-300"
FDA Adverse Event
Injury
·OLYMPUS WINTER & IBE GMBH BERLIN FACILITY·Product code GEI·November 30, 2022