30 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ALAMO T
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04064984699557·GENUMEDI PSS BLUE SIZE III
Bernafon
FDA UDI
Bernafon AG·05711584052488·JU7 ITCD, WL R BE JUNA 7
PRINCETON
FDA UDI
Princeton Medical Group, Inc.·00810158216709·FORCEPS JEWELER FIG. 3 .3MM TIP 4.75"
ADSON TISSUE FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896076433·ADSON TISSUE FORCEPS WITH TUNGSTEN CARBIDE PLAT...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197053020·DANDY Hemostatic Forceps,1x2 teeth
140mm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197053037·Moynihan delicate artery forceps, cvd.
150mm, 6"
ANGIOSCULPT PTA SCORING BALLOON CATHETER MODEL 2039-XXYY, 2076-XXYY, 2092-XXYY, 2105-XXYY
FDA 510(k)
FDA Class 2
·Cardiovascular
59% EXTREME H2O (HIOXIFILCON A) SOFT CONTACT LENS
FDA 510(k)
FDA Class 2
·Ophthalmic
STRATUS CS
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code DAP·November 11, 2015
LOGIC FEMORAL PS POR RIGHT SZ 2
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 10, 2025
STRATUS CS
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code DAP·November 9, 2015
RESTORE ADVANCED
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 31, 2013
LIFEVEST WCD 3000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·June 15, 2011
2250051-2008-00286
FDA Adverse Event
Malfunction
·Product code KSZ·June 12, 2008
BD VACUTAINER® MULTIPLE SAMPLE LUER ADAPTER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 24, 2021
SYRINGE 5ML SALINE FILL CHINA SP
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code NGT·October 17, 2023
BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET PRE-ATTACHED HOLDER
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·April 14, 2026
LOGIC CR FEMORAL POR, LEFT, SZ 3.5
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·December 11, 2024
BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·December 20, 2023