50 results
·
20ms
·
Sources: EU EUDAMED, US FDA
INVACARE POWERED WHEELCHAIRS, MODELS M50, M51, M71 & M91
FDA 510(k)
FDA Class 2
·Physical Medicine
CD HORIZON® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074034461·BONE SCREW 7021680 10 DEG ILC 6.5X80 SS
36PW - Norfolk Southern 002168-0 - Poly White
FDA UDI
Certified Safety Manufacturing, Inc.·00766588170060·36PW - Norfolk Southern 002168-0 - Poly White
PROWLER SELECT 10 AND 14 INFUSION CATHETERS WITH AND WITHOUT PRE-SHAPED TIPS
FDA 510(k)
FDA Class 2
·Cardiovascular
NONCOR INFUSION SETS; NONCOR PORT INFUSION SETS
FDA 510(k)
FDA Class 2
·General Hospital
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·August 4, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·August 4, 2017
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0216808276338217201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF021680827631317201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF021680827633217201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0216808276315917201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0216808276312017201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0216808276338117201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0216808276312717201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF021680827631217201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF021680827632517201·BTE-TRT
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·February 7, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·February 7, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·October 31, 2019
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·March 30, 2019