36 results · 20ms · 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.

SODEM HIGH SPEED SYSTEM (PNEUMATIC)

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

AOS CANCELLOUS LOCKING SCREW 4.0mm x 70mm

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665008708·

Oph. Cystotomes

FDA UDI
KATENA PRODUCTS, INC.·00841668113714·CYSTOTOME REVERSED FORM 25GA

ETHIBOND EXCEL VALVE LOOP SUTURE

FDA 510(k)
FDA Class 2 ·Cardiovascular

JAMSHIDI BIOPSY NEEDLE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

NONE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·September 3, 2008

SYNCHRO 14 NEURO GUIDEWIRE

FDA Adverse Event
Injury ·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORPORATION·Product code DQX·July 24, 2007

SYNCHRO -10 NEURO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIV·Product code DQX·December 15, 2006

SYNCHRO-14 NEURO GUIDEWIRE

FDA Adverse Event
Malfunction ·NEUROVASCULAR , A DIV. OF BOSTON SCIENTIFIC CORP·Product code DQX·December 19, 2006

SYNCHRO 14 GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP.·Product code DQX·September 20, 2007

SYNCHRO .014 GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP. / NEUROCASCULAR DIVISION·Product code DQX·August 16, 2007

SYNCHRO .014 GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP. / NEUROVASCULAR DIV.·Product code DQX·August 16, 2007

SYNCHRO -14 NEURO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIVISION·Product code DQX·November 30, 2006

SYNCHRO-14 NEURO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code DQX·September 12, 2007

SYNCHRO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQX·October 16, 2009

OMNIPOD INSULIN PUMP

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code LZG·February 26, 2013

STENOSCOP

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEM (INDIA) PRIVATE LTD. (GE PRIVATE)·Product code JAA·February 24, 2011

COLLEAGUE CX VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·April 3, 2008

SYNCHRO 14 "S" NEURO GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP.·Product code DQX·September 20, 2007

SYNCHRO 10 NEURO GUIDEWIRE

FDA Adverse Event
Injury ·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code DQX·November 7, 2007