1,080 results · 19ms · 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.

DRILL GUIDE EXTENSION

FDA UDI
Biomet Orthopedics, LLC·00887868074950·

IMMULITE® 2000 Systems DGX Digoxin

FDA UDI
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD·00630414961286·Digoxin - IMMULITE - RGT - 200 Tests

THYMATRON DGX

FDA Adverse Event
Injury ·SOMATICS INC·Product code GXC·May 7, 2001

MECTA CORPORATION

FDA Adverse Event
Injury ·Product code GXC·March 22, 2019

SOMATICS THYMATRON DGX

FDA Adverse Event
Malfunction ·SOMATICS·Product code GXC·December 8, 1999

MECTA SPECTRUM 5000Q UNIT

FDA Adverse Event
Injury ·MECTA·Product code GXC·January 28, 2017

LUSEE WIRE GUIDE WIRE

FDA Adverse Event
Malfunction ·CORDIS CORP.·Product code DGX·July 24, 1995

THYMATRON

FDA Adverse Event
Injury ·SOMATICS, LLC.·Product code QGH·April 23, 2024

VITROS CHEMISTRY PRODUCTS PHYT SLIDES

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code DIP·November 9, 2021

Ng1m(A), Antigen, Antiserum, Control

FDA classification
FDA Class 1 ·Ng1m(A), Antigen, Antiserum, Control

TiLite

FDA UDI
Tilite·00853316008075·

DAX EYEWEAR

FDA registration
DAX EYEWEAR·1 product·🇺🇸 United States

SOLO-DEX

FDA registration
SOLO-DEX·1 product·🇺🇸 United States

CGX, LLC

FDA registration
CGX, LLC·2 products·🇺🇸 United States

PRO-DEX, INC.

FDA registration
PRO-DEX, INC.·9 products·🇺🇸 United States

Pro-Dex Inc

FDA registration
Pro-Dex Inc·9 products·🇺🇸 United States

Coalition AGX Plate and Coalition AGX Spacer

FDA 510(k)
FDA Class 2 ·Orthopedic

IMD 7GX

FDA 510(k)
FDA Class 1 ·Dental

Arm Monopolar hook

FDA UDI
DEX SURGICAL·03665772000091·The monopolar hook are reusable (40 uses) endos...

Monopolar protection sleeve

FDA UDI
DEX SURGICAL·03665772000046·Monopolar protection sleeve is designed to be i...