16 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NeoMatriX Wound Matrix
FDA 510(k)
FDA Unclassified
·Unknown
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376484198·Pelvic Posterior Paddle
CAREVENT PAR (PUBLIC ACCESS RESUSCITATOR)
FDA 510(k)
FDA Class 2
·Anesthesiology
MIDWEST REPROCESSING CENTER REPROCESSED SCD EXPRESS SLEEVES/ FOOT CUFFS, MIDWEST REPROCESSING CENTER REPROCESSED ALP SLE
FDA 510(k)
FDA Class 2
·Cardiovascular
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 17, 2014
TRIDENT HEMISPHERICAL CLUSTER HOLE SHELL
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·June 21, 2013
GENESIS 8-CHANNEL RECHARGEABLE IPG
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 21, 2011
LACTO SCR 2.0X7MM 2.0 SYS 2/PK
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code JEY·December 15, 2021
L-PLT LT REG 2.0 LACTOSORB SYS
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HRS·December 15, 2021
LACTO SCR 2.0X7MM 2.0 SYS 2/PK
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code JEY·December 15, 2021
LACTO SCR 2.0X7MM 2.0 SYS 2/PK
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code JEY·December 15, 2021
LACTO SCR 2.0X7MM 2.0 SYS 2/PK
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code JEY·December 16, 2021
LACTO SCR 2.0X7MM 2.0 SYS 2/PK
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code JEY·December 15, 2021
LACTO SCR 2.0X7MM 2.0 SYS 2/PK
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code JEY·December 15, 2021
LACTO SCR 2.0X7MM 2.0 SYS 2/PK
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code JEY·December 15, 2021
LACTO SCR 2.0X7MM 2.0 SYS 2/PK
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code JEY·December 15, 2021