24 results · 22ms · Sources: EU EUDAMED, US FDA

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Tria Firm Ureteral Stent

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

Phasix

FDA UDI
Davol Inc.·00801741010637·Phasix Plug and Patch, Extra Large

Hayden Medical

FDA UDI
Hayden Medical, Inc.·00840319705636·Andrews-Pynchon Suction Tube 10" (25cm), delica...

Marina Medical

FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306804779·Desmarres Chalazion Clamp, Large, 17mm x 28mm

RS SAFE BLUE NITRILE MEDICAL EXAMINATION GLOVES (POWDER FREE)

FDA 510(k)
FDA Class 1 ·General Hospital

BARCO 5MP MAMMO, MODEL MDMG-5221

FDA 510(k)
FDA Class 2 ·Radiology

CARDINAL HEALTH

FDA Adverse Event
Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 12, 2024

CARDINAL HEALTH

FDA Adverse Event
Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 12, 2024

CARDINAL HEALTH

FDA Adverse Event
Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 12, 2024

CARDINAL HEALTH

FDA Adverse Event
Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 12, 2024

CARDINALHEALTH

FDA Adverse Event
Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 13, 2024

CARDINALHEALTH

FDA Adverse Event
Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 13, 2024

CARDINALHEALTH

FDA Adverse Event
Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 13, 2024

CARDINALHEALTH

FDA Adverse Event
Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 13, 2024

CYPHER SIROLIMUS-ELUTING CORONARY STENT

FDA Adverse Event
Malfunction ·CORDIS DE MEXICO·Product code NIQ·October 6, 2008

POWER PRO AMBULANCE COT

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·June 26, 2013

ECLIPSE

FDA Adverse Event
Malfunction ·VARIAN MEDICAL SYSTEMS FINLAND OY·Product code MUJ·July 27, 2011

CARDINALHEALTH

FDA Adverse Event
Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 13, 2024

NSK

FDA Adverse Event
Injury ·NAKANISHI INC.·Product code EGS·June 21, 2019

BD MAX¿ CPO

FDA Adverse Event
Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·May 13, 2025