1,213 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LZI Oxycodone III Enzyme Immunoassay
FDA 510(k)
FDA Class 2
·Clinical Toxicology
E-A-RLINK™
FDA UDI
3M COMPANY·00080529510167·3M(TM) E-A-RLINK(TM) 3B Foam Eartip pediatric ...
OSE
FDA UDI
ORTHODONTIC SUPPLY & EQUIPMENT COMPANY INC·00810042124745·EXPANDO RETRACTOR - SMALL #1
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193113395·HA PEEK EVOS Straight, ,7mmx8mmx 30mm , FLAT 0...
Ophthlamic Speculum
FDA UDI
KATENA PRODUCTS, INC.·10841668115159·BARRAQUER SPECULUM Disposable with Finger tabs ...
24M - Memphis Light & Gas - Metal
FDA UDI
Certified Safety Manufacturing, Inc.·00766588000077·24M - Memphis Light & Gas - Metal
A-CIFT® SoloFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361023678·A-CIFT SOLOFUSE IBFD, Lordotic 13mm Long, 17mm ...
SULZER VASCUTEK GELSOFT ERS VASCULAR PROSTHESIS
FDA 510(k)
FDA Class 2
·Cardiovascular
LIBERTY 5000 BREAST COIL WITH DISPOSABLE BIOPSY PLATES
FDA 510(k)
FDA Class 2
·Radiology
INTIMA-II Y 24GAX0.75IN PRN/EC SLM
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·January 13, 2021
PUMP MMT-1780KPK 670G PATHWAY BLACK MG
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·July 18, 2022
HEART LUNG MACHINE
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code KFM·April 27, 2020
PROXIMATE ILS CIRCULAR STAPLER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·October 27, 2014
MAXIMO VR
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code LWS·August 11, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 2, 2013
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON LABORATORIES, INC. / HUNTINGTON·Product code HQL·October 18, 2007
HEART LUNG MACHINE
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code KFM·May 14, 2020
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON LABORATORIES, INC/ HUNTINGTON·Product code HQL·October 18, 2007
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·January 7, 2020
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON LABORATORIES, INC.·Product code HQL·July 19, 2007