37 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
3M Attest Rapid Readout Biological Indicator 1295
FDA 510(k)
FDA Class 2
·General Hospital
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741520600·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674152060060·
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704283488·KLEINERT-KUTZ HOOK 6" 3 MILLIMETER
Epredia
FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693063760·The blades and knifes consumables are for use w...
Sklar®
FDA UDI
SKLAR CORPORATION·10649111251566·OP SCISS 6" CVD BL/BL
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100172·KRATZ WIRE SPECULUM WITH WINGS
RADIANCE
FDA 510(k)
FDA Class 2
·Radiology
OPTI-AMP DC-POWERED
FDA 510(k)
FDA Class 2
·Neurology
Truliant
FDA UDI
Exactech, Inc.·10885862523358·PS NOTCH GUIDE, SIZE 6
Herbert/Whipple®
FDA UDI
Zimmer, Inc.·00889024033986·
BD VACUTAINER® SST¿ II ADVANCE PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·February 11, 2025
CAPSURE SP 4024
FDA Adverse Event
Injury
·MPRI·Product code DTB·June 7, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011
IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code EZW·October 8, 2014
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 30, 2022
BD INSYTE AUTOGUARD
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·January 20, 2025
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·March 18, 2026
METACROSS OTW PTA BALLOON DILATATION CATHETER
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 19, 2019
OHICHO NEO
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·February 7, 2024