25 results · 26ms · Sources: EU EUDAMED, US FDA

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HEMOSIL PROTEIN C

FDA 510(k)
FDA Class 2 ·Hematology

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X0624300·6mm H x 24mm W x 30mm L x 0 degrees XLIF

OsteoMed

FDA UDI
OSTEOMED LLC·00845694008457·2.4mm x 30mm Lag Screw

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X06243080·6mm H x 24mm W x 30mm L x 8 degrees XLIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587L062430120·6mm H x 24mm W x 30mm L XLIF Trial 12 degree Lo...

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X062430120·6mm H x 24mm W x 30mm L x 12 degrees XLIF

OsteoMed

FDA UDI
OSTEOMED LLC·00845694035187·2.4 x 30mm Lag Screw, Sterile

OsteoMed

FDA UDI
OSTEOMED LLC·00845694067089·HPS 2.4 x 30mm Lag Screw Sterile Qty 5

MULTI-METER GLUCOSE CALIBRATION VERIFICATION MATERIAL, MODEL RNA GL3

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

ISO FUNCTIONAL

FDA 510(k)
FDA Class 2 ·Dental

SOL-MILLENNIUM

FDA Adverse Event
Malfunction ·SOL-MILLENNIUM MEDICAL INC·Product code FMF·May 16, 2025

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 16, 2013

RUSCH ENDOTRACHEAL TUBE AGT ORAL CUFFED 7.5MM

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code BTR·March 18, 2011

S5

FDA Adverse Event
Malfunction ·SORIN GROUP, USA, INC.·Product code DTQ·May 31, 2008

S-ROM M HEAD 36MM +0

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code JDI·March 21, 2012

PINNACLE MTL INS NEUT36IDX60OD

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 21, 2012

S-ROM M HEAD 36MM +0

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code JDI·March 21, 2012

PINNACLE MTL INS NEUT36IDX60OD

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 21, 2012

PINNACLE SECTOR II CUP 60MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 26, 2013

PINN CAN BONE SCREW 6.5MMX45MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code NDJ·August 26, 2013