40 results · 40ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

AVALON ELITE VASCULAR ACCESS KIT

FDA 510(k)
FDA Class 2 ·Cardiovascular

EQUASHIELD SYSTEM PROTECTIVE PLUS

FDA 510(k)
FDA Class 2 ·General Hospital

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

NIPRO BLOOD TUBING SET W/TP

FDA Adverse Event
Malfunction ·NIPRO (THAILAND) CORP. LTD.·Product code FJK·February 6, 2024

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 6, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 4, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

NIPRO BLOOD TUBING SET W/TP

FDA Adverse Event
Injury ·NIPRO (THAILAND) CORP. LTD.·Product code FJK·January 17, 2024