33 results · 21ms · Sources: EU EUDAMED, US FDA

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INTEGRA FREEDOM WRIST ARTHROPLASTY SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B16741322500·

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B1674132250060·

Modelstar S

FDA UDI
S & S Scheftner GmbH·04260207850198·Ingots, 250g

Clear Readers

FDA UDI
Diversified Products, Inc.·00037741113263·

Clear Readers

FDA UDI
Diversified Products, Inc.·00842894113905·

CHX=CHX PLUS

FDA 510(k)
FDA Unclassified ·Unknown

GEOFORM ANNULOPLASTY RING, MITRAL MODEL 4200

FDA 510(k)
FDA Class 2 ·Cardiovascular

IMP TM 4.7MM MTX FULL, 11.5MM

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·June 27, 2024

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·March 3, 2026

FUJIFILM 600 SERIES ENDOSCOPE EC-600WM

FDA Adverse Event
Malfunction ·FUJIFILM CORPORATION·Product code FDF·January 22, 2025

530G INSULIN PUMP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code OZO·October 1, 2014

SD/PD LONG CURVED

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·May 29, 2013

E360 VENTILATOR

FDA Adverse Event
NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·June 3, 2011

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·October 7, 2025

IMP TM 4.7MM MTX FULL, 10

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·October 30, 2024

IMP TM 6.0MM MTX FULL, 10

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·June 29, 2023

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·February 24, 2026

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·February 24, 2026

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·February 24, 2026