54 results · 19ms · Sources: EU EUDAMED, US FDA

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DIAGNOSTIC ULTRASOUND SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

NexxZr™ T / D-100-16-NT-B100-SD

FDA UDI
SAGEMAX BIOCERAMICS, INC·00842271112699·

Zavation

FDA UDI
Zavation LLC·00842166108264·PLIF 11x32x5deg -9

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970010·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970027·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172974018·UniTip High Resolution Catheter 10F

AUTOCLAVABLE CAMER HEAD MODEL OTV-Y0017

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

MODIFICATION TO MACS MODULAR ANTERIOR CONSTRUCT SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAVED KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·April 12, 2024

LASSO 2515 NAV VARIABLE CATHETER

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·May 29, 2013

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·June 16, 2011

UNKNOWN PRODUCT

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·August 21, 2008

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAVED KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·July 18, 2025

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 4, 2025