10 results
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26ms
·
Sources: EU EUDAMED, US FDA
RUSSIAN TISSUE FORCEPS, 6 + SS 410 OR 420
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Kwik Kleen
FDA UDI
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657072199·Kwik Kleen Kerrison 4mm x 180mm x 90 Deg
NAR Kit
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209110643·KIT, SAVE-A-LIFE 2 - CUSTOM
MODEL 3300E/ER MONOPLACE HYPERBARIC OXYGEN CHAMBER
FDA 510(k)
FDA Class 2
·Anesthesiology
8MP Color LCD Monitor, RadiForce RX850, RX850-AR
FDA 510(k)
FDA Class 2
·Radiology
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·October 4, 2010
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·November 30, 2012
PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) TTS TRACHEOSTOMY TUBE 7.0MM TIGHT TO SHAFT CUFF, Product Code/List Number/Item Code 670170; b) TTS TRACHEOSTOMY TUBE 8.0MM TIGHT TO SHAFT CUFF 1/EA, Product Code/List Number/Item Code 670180
FDA Enforcement
Class I
·Ongoing·Smiths Medical ASD Inc.·September 4, 2024
Pipeline Flex Embolization Device
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021