2,128 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STREPTOCOCCUS APP. SEROLOGICAL REAGENTS
FDA 510(k)
FDA Class 1
·Microbiology
ArgenZ HT+ 98x14 C1
FDA UDI
ARGEN CORPORATION, THE·D818122019·Dental porcelain/ceramic restoration kit
36M - Class B 21 - Metal
FDA UDI
Certified Safety Manufacturing, Inc.·00766588620190·36M - Class B 21 - Metal
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K1220100·Breaker, Extended Tab
RESTORATION ACETABULAR WEDGE AUGMENTS
FDA 510(k)
FDA Class 2
·Orthopedic
PERIFIX CATHETER CONNECTOR
FDA 510(k)
FDA Class 2
·Anesthesiology
UNKNOWN DEPUY FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. ? REG. # 8010379·Product code KWY·May 21, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 19, 2014
ASR UNI FEMORAL IMPL SIZE 45
FDA Adverse Event
Injury
·DEPUY INTL. LTD.·Product code KWA·June 9, 2011
BUBBLE GUPPIES
FDA Adverse Event
Injury
·ASO LLC·Product code KGX·October 10, 2019
BUBBLE GUPPIES
FDA Adverse Event
Injury
·ASO LLC·Product code KGX·October 10, 2019
CADD LEGACY PUMP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FRN·September 5, 2019
NUCLEUS CI522 COCHLEAR IMPLANT WITH SLIM STRAIGHT ELECTRODE
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·August 11, 2019
DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code PQF·March 1, 2019
NUCLEUS 24
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·August 11, 2019
NUCLEUS CI512 COCHLEAR IMPLANT WITH CONTOUR ADVANCE ELECTRODE
FDA Adverse Event
Malfunction
·COCHLEAR LTD·Product code MCM·April 1, 2019
8100 ALARIS PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·December 18, 2020
PRO ADVANTAGE
FDA Adverse Event
Injury
·ASO LLC·Product code KGX·March 14, 2019
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code EGS·April 1, 2019
GALILEO ECHO V2
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·April 26, 2019