10,000 results · 57ms · 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.

Quad Matrix System™

FDA UDI
GARRISON DENTAL SOLUTIONS, L.L.C.·00810038091167·Quad Wedge Orange Refill: 100 counts

Qor Labs

FDA UDI
LW SCIENTIFIC, INC.·00664816002780·10,000rpm Mini Centrifuge

Qor Labs

FDA UDI
LW SCIENTIFIC, INC.·00664816003510·10,000rpm Mini 10K Centrifuge

Qor Labs

FDA UDI
LW SCIENTIFIC, INC.·00664816002896·Pipette pump; 25ml

Qor Labs

FDA UDI
LW SCIENTIFIC, INC.·00664816003435·Slide Warmer (66-slide)

Qor Labs

FDA UDI
LW SCIENTIFIC, INC.·00664816005897·HemaRok Single Deck Rocker / Mixer; 30RPM, hold...

Qor Labs

FDA UDI
LW SCIENTIFIC, INC.·00664816005903·HemaRok Double Deck Rocker / Mixer; 30RPM, hold...

Qor Labs

FDA UDI
LW SCIENTIFIC, INC.·00664816003237·Slide Warmer (24-slide)

Qor Labs

FDA UDI
LW SCIENTIFIC, INC.·00664816003442·AT Digital Centrifuge, 8-Place Rotor, Fixed Speed

Qor Labs

FDA UDI
LW SCIENTIFIC, INC.·00664816002889·Pipette pump; 10ml

Quad Matrix System™

FDA UDI
GARRISON DENTAL SOLUTIONS, L.L.C.·00810038091204·Quad Wedge Orange Refill: 50 count

COAGUCHEK ® XS SYSTEM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·January 28, 2020

PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC MILACA, INC.·Product code LWP·June 10, 2014

BD PHASEAL¿ OPTIMA CONNECTOR (C35-O)

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·June 16, 2022

COAGUCHEK XS SYSTEM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·December 16, 2020

COAGUCHEK XS SYSTEM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·September 21, 2021

RESVENT IBREEZE 20A

FDA Adverse Event
Injury ·RESVENT MEDICAL TECHNOLOGY CO., LTD.·Product code QOR·August 21, 2024

RESVENT IBREEZE 20A

FDA Adverse Event
Injury ·RESVENT MEDICAL TECHNOLOGY CO., LTD.·Product code QOR·February 23, 2023

IBREEZE 25STA

FDA Adverse Event
Malfunction ·RESVENT MEDICAL TECHNOLOGY CO., LTD·Product code QOR·January 26, 2023

IBREEZE 20A

FDA Adverse Event
Injury ·RESVENT MEDICAL TECHNOLOGY CO., LTD.·Product code QOR·March 28, 2023