36 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KJ SUBMERGED SYSTEM
FDA 510(k)
FDA Class 2
·Dental
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814732·GENUMEDI EXTRA WIDE SAND SIZE V
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814725·GENUMEDI EXTRA WIDE SAND SIZE IV
Dornier MedTech
FDA UDI
Dornier MedTech GmbH·04049957003265·Gemini Lithotripter, 65 KW
ADSON HARRIS FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896053526·ADSON HARRIS FORCEPS TUNGSTEN CARBIDE DUST RING...
M2A 38MM INSERTER PLATE MULTITOOL
FDA UDI
Biomet Orthopedics, LLC·00880304441644·
LEONE SPA
FDA UDI
LEONE SPA·08033707081814·IMPLANT MAX STABILITY W/CAP D3,75 L10MM
LEONE SPA
FDA UDI
LEONE SPA·08033707092605·IMPLANT MAX STABILITY W/CAPS D3,75 L8MM
K2M General Instruments
FDA UDI
VB Spine LLC·10888857520301·Split Tube Retractor, Size Ø12x120 mm
ELECSYS C-PEPTIDE CALCHECK 5
FDA 510(k)
FDA Class 1
·Clinical Chemistry
CARDIOVASCULAR ARRAY
FDA 510(k)
FDA Class 2
·Radiology
NC TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Injury
·ABBOTT VASCULAR·Product code LOX·December 16, 2022
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 9, 2013
530G INSULIN PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OZO·September 19, 2014
NI
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·May 18, 2011
TREK¿
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR INC.·Product code LOX·May 27, 2025
40MM I.D. SIZE LL NEUTRAL LINER USE WITH 58MM O.D. SIZE LL SHELL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·July 3, 2024
TREK¿
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR INC.·Product code LOX·January 7, 2026
MICRUSFRAME10 5MM X 17CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022
GALAXY G3 XSFT 4MM X 10CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2022