174 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Kerecis Reconstruct
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Invisalign Cheek Retractor, Medium
FDA UDI
Align Technology, Inc.·00816063021131·Cheek Retractor
Blade Scalpel
FDA UDI
KATENA PRODUCTS, INC.·00841668113448·SUPER SHARPS 15 DEG 3MM (BX/5)
Blade Scalpel
FDA UDI
KATENA PRODUCTS, INC.·00841668113561·IMPLANT BLADE 6.2MM (BX/5)
EXPERIENCE®
FDA UDI
Gc Orthodontics America Inc.·D78820243000201·EXP MBT 022/UR3 -7T 8A
EXPERIENCE®
FDA UDI
Gc Orthodontics America Inc.·D78820243000301·EXP XT 022/LR3 -3T 7A 2R
EXPERIENCE®
FDA UDI
Gc Orthodontics America Inc.·D78820243000101·EXP ROTH 022/LR3 -11T 7A 2M
TYCO ELECTRONICS ELECTROCARDIOGRAPH (ECG) LEADWIRE SET
FDA 510(k)
FDA Class 2
·Cardiovascular
ISO FUNCTIONAL
FDA 510(k)
FDA Class 2
·Dental
BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code QJR·August 28, 2020
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 11, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 9, 2024
INFUSION DEVICES - UNKNOWN
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 30, 2024
AUTOSOFT 30
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 4, 2024
INFUSION DEVICES - UNKNOWN
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 30, 2024
AUTOSOFT 30
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 4, 2024
AUTOSOFT 30
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 4, 2024
TAXUS? LIBERTÉ?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·October 27, 2014
DST SERIES EEA ORVIL 25MM DEVICE
FDA Adverse Event
Injury
·UNITED STATES SURGICAL·Product code GDW·August 5, 2011
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 2, 2013