63 results · 39ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

BRACCO DIAGNOSTICS INC. PROTOCO, L TOUCH COLON INSUFFLATOR

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

NexxZr™ T / D-100-18-NT-OM20-SD

FDA UDI
SAGEMAX BIOCERAMICS, INC·00842271114020·

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613114916·Metzenbaum (Lahey) Scissors, TC, Straight, Deli...

PRE-VACUUM AUTOCLAVE WITH STEAM GENERATOR AND VERTICAL SLIDING DOOR, MODELS 4472 EP-1V AND 5596 EP-1V

FDA 510(k)
FDA Class 2 ·General Hospital

INDISCAL DIGITAL MANOMETER

FDA 510(k)
FDA Class 2 ·General Hospital

M.U.S.T. PEDICLE SCREW 7X45

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MNI·January 20, 2017

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

INCEPTA

FDA Adverse Event
Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 1, 2014

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

IN TOUCH ZU

FDA Adverse Event
Injury ·STRYKER MEDICAL·Product code FNL·June 13, 2011

FLEXOR RADIAL ACCESS SET

FDA Adverse Event
Injury ·COOK, INC.·Product code DYB·April 13, 2015

PEDICLE SCREW 03.50.030 PEDICLE SCREW 7X40

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·February 3, 2020

MECTALIF POSTERIOR

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·October 8, 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-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