34 results · 28ms · Sources: EU EUDAMED, US FDA

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PEDIATRIC FIXATION RODS

FDA 510(k)
FDA Class 2 ·Orthopedic

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·H65890007641·HP Mixing Tips Small Yellow

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·10304040061364·Compo-Post Medium

PowerPICC Provena

FDA UDI
Bard Access Systems, Inc.·00801741141720·Catheter Placement Kit

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·10304040051853·HP Mixing Tip Yellow Small 4.2mm

ASIA MED

FDA UDI
asia-med GmbH·04251282513481·asia-med Special+ No. 12: coated acupuncture n...

ASIA MED

FDA UDI
asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282506469·asia-med Special+ No. 12: coated acupuncture n...

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL UM-D·Product code FPA·March 19, 2025

COMPLETE BRAND COMFORTPLUS MULTI-PURPOSE SOLUTION

FDA 510(k)
FDA Class 2 ·Ophthalmic

ACCU-CHEK COMPLETE METER

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·May 6, 2022

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2022

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2022

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2022

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2022

LUMIRADX SARS-COV-2 AG TEST STRIP KIT

FDA Adverse Event
Malfunction ·LUMIRADX UK LTD.·Product code QKP·February 25, 2022

AUTOSOFT 90

FDA Adverse Event
Malfunction ·UNOMEDICAL UM-D·Product code FPA·March 19, 2025

INTERSTIM

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·June 10, 2016

UNKNOWN TROFIX TROCHANTERIC FIXATION PLATE

FDA Adverse Event
Injury ·ZIMMER SWITZERLAND MANUFACTURER GMBH·Product code KTT·August 22, 2023

UNKNOWN TROFIX TROCHANTERIC FIXATION PLATE

FDA Adverse Event
Injury ·ZIMMER SWITZERLAND MANUFACTURER GMBH·Product code KTT·August 22, 2023