10,000 results
·
30ms
·
Sources: EU EUDAMED, US FDA
ASTORA MINIARC PRO SLING SYSTEM
FDA Adverse Event
Injury
·ASTORIA WOMEN'S HEALTH LLC·Product code PAH·January 8, 2017
MiniArc Pro Single incision Sling System, Model number / Product Reference 9000261, Lot 936405xxx. Designed to treat female stress urinary incontinence.
FDA Recall
Terminated
·Astora·Product code PAH·October 26, 2015
MiniArc Pro Single incision Sling System, Model number / Product Reference 9000261, Lot 936405xxx. Designed to treat female stress urinary incontinence.
FDA Enforcement
Class II
·Terminated·Astora·November 25, 2015
AMS ELEVATE ANTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTP·July 1, 2015
AMS ELEVATE PC ANTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTP·July 17, 2015
AMS ELEVATE ANTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTP·September 14, 2015
AMS ELEVATE ANTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTP·August 13, 2015
AMS MONARC SLING SYSTEM
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTN·September 14, 2015
AMS ELEVATE POSTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTP·September 18, 2015
AMS ELEVATE PC ANTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTP·July 17, 2015
AMS MINIARC PRO SINGLE INCISION SLING SYSTEM
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code PAH·December 19, 2014
AMS ELEVATE PC ANTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTP·July 16, 2015
AMS ELEVATE ANTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTP·July 1, 2015
AMS ELEVATE POSTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTP·August 5, 2015
AMS ELEVATE POSTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTP·September 17, 2015
AMS ELEVATE ANTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTP·September 29, 2015
AMS RETROARC RETROPUBIC SLING SYSTEM
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTN·September 29, 2015
AMS MONARC SLING SYSTEM
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTN·August 31, 2015
AMS ELEVATE ANTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH (IRELAND)·Product code OTP·March 11, 2014
AMS ELEVATE PC ANTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
FDA Adverse Event
Injury
·ASTORA WOMEN'S HEALTH LLC·Product code OTP·October 31, 2014