7,701 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Needle-Free Valves
FDA UDI
ORIGEN BIOMEDICAL, INC.·10816203020120·Needle-free valve with caps, case of 10
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749077797·CERAMO punch with ejector flat foot, 40°upw., 3...
6ml Syringe, NFV x SCD
FDA UDI
ORIGEN BIOMEDICAL, INC.·10816203020229·6ml syringe on a needle-free valve with 15cm SC...
NFV x SCD 50ml Syringe
FDA UDI
ORIGEN BIOMEDICAL, INC.·10816203020212·60ml syringe on a needle-free valve with 15cm S...
TEXIUM CLOSE MALU LUER
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·August 20, 2019
TEXIUM CLOSED MALE LUER
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·August 20, 2019
MAXZERO NEEDLENESS CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·November 12, 2019
MAXZERO NEEDLENESS CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·November 12, 2019
MAXZERO NEEDLENESS CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·November 12, 2019
ALARIS PUMP MODULE ADMINISTRATION SET
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·November 18, 2019
MINIBORE TRI-FUSE SET
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·October 23, 2018
TEXIUM NEEDLE-FREE SYRINGE 10ML
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·January 27, 2020
ALARIS PUMP MODULE ADMINISTRATION SET
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·November 18, 2019
ANALYTICAL P MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NFV·September 5, 2013
BENZODIAZEPINES
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NFV·October 11, 2013
Alpha-Omega Services, Inc. Product No: SPECIAL-NFV Description: CUSTOM FLEXIGUIDE NEEDLE, SERIES 15, WITH FEMALE LUER AND STYLET WITH MALE LUER 28CM, SET OF 100 Quantity: 1/PKG Lot No: K00136 L-SPECIAL- NFV. The FlexiGuide is a flexible needle designed to provide an enclosed pathway for localized radiation therapy using a Remote High Dose Rate (HDR) Afterloader or manual Low Dose Rate (LDR) method.
FDA Recall
Terminated
·Alpha Omega Services Inc·Product code IWJ·November 15, 2007
HOMECHOICE CYCLER-REFURBISHED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·August 23, 2007
Test, Benzodiazepine, Over The Counter
FDA classification
FDA Class 2
·Test, Benzodiazepine, Over The Counter
DFV Desensitizing Varnish-Strawberry Flavor, DFV Desensitizing Varnish-Bubblegum (Tutti-Fruity) Flavor, DFV Desensitizing Varnish-Spearmint Flavor, DFV Desensitizing Varnish-Chocolate Flavor, DFV Desensitizing Varnish-Marshmallow Flavor
FDA 510(k)
FDA Class 2
·Dental
MagBio Genomics, Inc.
FDA UDI
Magbio Genomics, Inc.·00850045030353·Viral RNA isolation - KingFisher MVP II Alterna...