2,422 results · 31ms · Sources: EU EUDAMED, US FDA

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Renamic PGH

FDA UDI
BIOTRONIK SE & Co. KG·04035479114510·

Renamic PGH ICD

FDA UDI
BIOTRONIK SE & Co. KG·04035479114527·

GRAFTOLOGER PGH & ACL RECONSTRUCTION INSTRUMENT SET

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

BIFURCATED GORE-TEX STRETCH VASCULAR GRAFT

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code DSY·March 30, 2020

Western/Scott Fetzer

FDA UDI
Western Enterprises·B929M1346PGH0·M1 ADJ.REG 0-100 PSI/CGA346/HT

Western/Scott Fetzer

FDA UDI
Western Enterprises·B929M1540PGH0·M1 ADJ.REG 0-100 PSI/CGA540/HT

Western/Scott Fetzer

FDA UDI
Western Enterprises·B929M1320PGH0·M1 ADJ.REG 0-100 PSI/CGA320/HT

Western/Scott Fetzer

FDA UDI
Western Enterprises·B929M1326PGH0·M1 ADJ.REG 0-100 PSI/CGA326/HT

Western/Scott Fetzer

FDA UDI
Western Enterprises·B929M1580PGH0·M1 ADJ.REG 0-100 PSI/CGA580/HT

Western/Scott Fetzer

FDA UDI
Western Enterprises·B929M1500PGH0·M1 ADJ.REG 0-100 PSI/CGA500/HT

BIFURCATED GORE-TEX STRETCH VASCULAR GRAFT

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code DSY·March 30, 2020

BIFURCATED GORE-TEX STRETCH VASCULAR GRAFT

FDA Adverse Event
Death ·W.L. GORE & ASSOCIATES·Product code DSY·March 30, 2020

TO GORE-TEX® STRETCH VASCULAR GRAFT

FDA Adverse Event
Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021

GORE EXCLUDER AAA ENDOPROSTHESIS

FDA Adverse Event
Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·July 27, 2021

GORE-TEX® STRETCH VASCULAR GRAFT

FDA Adverse Event
Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021

ILIVIA 7 HF-T QP DF4 IS4 PROMRI

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code NIK·July 7, 2021

ELUNA 8 DR-T PROMRI

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code NVZ·July 13, 2020

BIFURCATED GORE-TEX STRETCH VASCULAR GRAFT

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code DSY·March 30, 2020

ICS 3000 PGH ICD

FDA Adverse Event
Other ·BIOTRONIK SE & CO. KG·Product code NVZ·April 2, 2012

ICS 3000

FDA Adverse Event
Other ·BIOTRONIK GMBH AND CO.·Product code KRG·October 20, 2005