63 results · 24ms · Sources: EU EUDAMED, US FDA

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GRI-BAG, GRI-BAG AP

FDA 510(k)
FDA Class 2 ·General Hospital

Baltic Denture System BDLoad

FDA UDI
Merz Dental GmbH·D7091033916·Baltic Denture System BDLoad BDLoad Lw6 PLSEbi...

INSTANT-VIEW Multi-Drugs of Abuse Urine Test AMP, BAR, BZD, COC, MET1000, MOR200

FDA UDI
ALFA SCIENTIFIC DESIGNS, INC.·10796918001358·INSTANT-VIEW Multi-Drugs of Abuse Urine Test AM...

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0330160·Coronal Bender, Right

DERMALIFE HYDROFUSION SKIN & BODY CARE SYSTEM

FDA 510(k)
FDA Class 2 ·Physical Medicine

MELKER EMERGENCY CRICOTHYROTOMY CATHETER SET

FDA 510(k)
FDA Class 2 ·Anesthesiology

R90 SPACERS

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MQP·October 9, 2009

R90 SPACERS

FDA Adverse Event
Other ·WARSAW ORTHOPEDIC INC·Product code MAX·November 6, 2009

R90 SPACERS

FDA Adverse Event
Injury ·SOFAMOR DANEK DEGGENDORF GMBH·Product code MAX·December 21, 2009

AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code FNL·April 3, 2013

TRAUMA TRANSTAR

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FPO·March 23, 2011

MULTI-LINK RX VISION CORONARY STENT SYSTEM

FDA Adverse Event
Death ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·April 24, 2008

PROGREAT

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·May 7, 2026

PROGREAT

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·May 7, 2026

PORTASCAN

FDA Adverse Event
Malfunction ·MEDIWATCH UK LTD·Product code ITX·November 17, 2011

PROGREAT

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQO·April 10, 2026

PROGREAT

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQO·May 7, 2026

PROGREAT

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·May 26, 2026

R90 SPACER

FDA Adverse Event
Malfunction ·MSD DEGGENDORF MFG·Product code NKB·August 5, 2011

PROGREAT

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 28, 2025