2,015 results · 22ms · Sources: EU EUDAMED, US FDA

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Eusol-C

FDA 510(k)
FDA Unclassified ·Unknown

36M - Loisville Gas & Electric - Metal

FDA UDI
Certified Safety Manufacturing, Inc.·00766588120133·36M - Loisville Gas & Electric - Metal

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613054472·Instrument Guards, Clear, Vented, 7/64" x 3/4

Avalign

FDA UDI
Avalign Technologies, Inc.·00190776020446·Keyhole Bracket

Avalign

FDA UDI
Avalign Technologies, Inc.·00190776119843·Keyhole Bracket, hole opening 25mm (1"), silico...

Endo-Model Standard Knee Prosthesis System

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575222230·Sparepart Kit Boxes for Endo-Model SL

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776116392·Keyhole Bracket

Endo-Model Standard Knee Prosthesis System

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575222070·Sparepart Kit Boxes for Endo-Model SL

Straight Pin 3.15 x 63 mm

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215046118·

CELLSEARCH CIRCULATING TUMOR CELL KIT

FDA 510(k)
FDA Class 2 ·Immunology

DIGITAL RETINAL CAMERA

FDA 510(k)
FDA Class 2 ·Ophthalmic

7900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·June 3, 2013

TRABECULAR METAL FEMORAL STEM

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code LPH·July 11, 2011

ANALYTICAL E MODULE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·October 10, 2014

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·December 27, 2013

NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Malfunction ·COCHLEAR LTD·Product code MCM·June 14, 2013

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·December 30, 2013

NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Injury ·COCHLEAR LTD.·Product code MCM·November 2, 2012

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·December 29, 2013

ADVIA Centaur Vitamin D Calibrator 2-pack; Reference Number:10493589. For use in the quantitative determination of Vit D.

FDA Enforcement
Class II ·Terminated·Siemens Healthcare Diagnostics, Inc·April 24, 2013