18 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RUSCH BLAKEMORE 3 LUMEN, STERILE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AXSOS
FDA UDI
Stryker GmbH·07613327095241·X-Ray Template
Polystar Selection EDITION
FDA UDI
Merz Dental GmbH·D7091981203·anteriors; shade B3; mould BIM6
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79812031·Sprint II Bracket McLaugh/Benn/Trev. .018" mand...
Symmetry Surgical®
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482086605·Symmetry® Forceps, Maxi Fenestrated, Ratcheting...
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79812030101·Sprint II Bracket McLaugh/Benn/Trev. .018" mand...
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79812030051·Sprint II Bracket McLaugh/Benn/Trev. .018" mand...
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79812031001·Sprint II Bracket McLaugh/Benn/Trev. .018" mand...
ENDOPATH ETS
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code KOG·March 18, 1998
Juliet Ti
FDA 510(k)
FDA Class 2
·Orthopedic
OB TRACEVUE OBSTETRICAL INFORMATION MANAGEMENT SYSTEM WITH RELEASE F.00
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
TX1 TISSUE REMOVAL SYS - MICROTIP
FDA Adverse Event
Malfunction
·AMERICAN OPTISURGICAL, INC.·Product code LFL·February 24, 2014
TX1 TISSUE REMOVAL SYS - MICROTIP
FDA Adverse Event
Malfunction
·AMERICAN OPTISURGICAL, INC.·Product code LFL·February 24, 2014
TX1 TISSUE REMOVAL SYSTEM - MICROTIP
FDA Adverse Event
Malfunction
·AMERICAN OPTISURGICAL, INC.·Product code LFL·February 24, 2014
TX1 TISSUE REMOVAL SYSTEM - MICROTIP
FDA Adverse Event
Malfunction
·AMERICAN OPTISURGICAL, INC.·Product code LFL·February 24, 2014
ACCU-CHEK ® SPIRIT
FDA Adverse Event
Injury
·ROCHE HEALTH SOLUTIONS INC·Product code LZG·February 27, 2013
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
Malfunction
·INVAMEX·Product code ILS·August 5, 2014
LINEAR HIP
FDA Adverse Event
Other
·ENCORE MEDICAL, L.P.·Product code LPH·January 26, 2011