45 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SPIRO PRO
FDA 510(k)
FDA Class 2
·Anesthesiology
PowerPICC
FDA UDI
Bard Access Systems, Inc.·00801741136511·Catheter Placement Kit
S NEEDLE
FDA UDI
asia-med GmbH·04251282511715·asia-med s-needle B-Type 2015: coated acupunct...
S NEEDLE
FDA UDI
asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282504724·asia-med s-needle B-Type 2015: coated acupunct...
GentleMax Pro Plus
FDA UDI
Candela Corporation·00817495023045·GMPP ACC Medium Spot Option Kit, w/Fiber Assembly
N/A
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024368064·SPREADER BAR DIAMETER 10MM X LENGTH 56CM
SEALOUETTE FIBRIN SEALANT EXTENDED DROPLET APPLICATOR, MODEL TE-1
FDA 510(k)
FDA Class 2
·General Hospital
RGP MULTI-PURPOSE SOLUTION ID 100136
FDA 510(k)
FDA Class 2
·Ophthalmic
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·March 18, 2025
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·June 13, 2024
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·June 13, 2024
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 30, 2025
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·March 18, 2025
SCREW LOCKING
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES OBERDORF·Product code HWC·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HRS·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·March 12, 2013
X8000 LIGHTSOURCE
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·February 3, 2011