12 results
·
19ms
·
Sources: EU EUDAMED, US FDA
ESOPHAGEAL MANOMETRY ANALYSIS MODULE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668112328·SURG-I-BAND GREEN
Eye Shield
FDA UDI
KATENA PRODUCTS, INC.·00841668111185·PIN HOLE EYE SHIELD WHITE PACK OF 12
P.S.M. SURGICAL HOOD
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HANSEN MEDICAL TRANSSEPTAL NEEDLE AND DILATOR
FDA 510(k)
FDA Class 2
·Cardiovascular
NexGen® Complete Knee Solution
FDA UDI
Zimmer, Inc.·00889024210684·
NexGen® Complete Knee Solution
FDA UDI
Zimmer, Inc.·00889024210677·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024445895·
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 24, 2021
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·January 30, 2013
EON MINI IPG, 16-CHANNEL RECHARGEABLE
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·January 12, 2011
OCTRODOE
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 15, 2014