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

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OKI Surgical Planning Software

FDA 510(k)
FDA Class 2 ·Radiology

OKI-YOSHITOMA HYDRODISS CAN 27 GA STR

FDA UDI
KATENA PRODUCTS, INC.·00841668140215·OKI-YOSHITOMA HYDRODISS CAN 27 GA STR

OKI-YOSHITOMA HYDRODISS CAN 27 GA 15 DEG

FDA UDI
KATENA PRODUCTS, INC.·00841668140222·OKI-YOSHITOMA HYDRODISS CAN 27 GA 15 DEG

OKI-YOSHITOMI HYDRODISS CAN 23 GA 45 DEG

FDA UDI
KATENA PRODUCTS, INC.·00841668140376·OKI-YOSHITOMI HYDRODISS CAN 23 GA 45 DEG

OKI-YOSHITOMA HYDRODISS CAN 27 GA 30 DEG

FDA UDI
KATENA PRODUCTS, INC.·00841668140239·OKI-YOSHITOMA HYDRODISS CAN 27 GA 30 DEG

OKI-YOSHITOMA HYDRODISS CAN 27 GA 45 DEG

FDA UDI
KATENA PRODUCTS, INC.·00841668140246·OKI-YOSHITOMA HYDRODISS CAN 27 GA 45 DEG

OKI-YOSHITOMI HYDRODISS CAN 23 GA 30 DEG

FDA UDI
KATENA PRODUCTS, INC.·00841668140369·OKI-YOSHITOMI HYDRODISS CAN 23 GA 30 DEG

OKI-YOSHITOMI HYDRODISS CAN 23 GA 25 DEG

FDA UDI
KATENA PRODUCTS, INC.·00841668140352·OKI-YOSHITOMI HYDRODISS CAN 23 GA 25 DEG

ST. JUDE

FDA Adverse Event
Other ·ST. JUDE·Product code DXY·January 8, 2012

AED PLUS

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·June 6, 2003

840 VENTILATOR

FDA Adverse Event
Malfunction ·COVIDIEN·Product code CBK·January 24, 2018

8015 ALARIS SYSTEM PC UNIT

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·January 13, 2021

CELL-DYN 1800 ANALYZER

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·December 5, 2012

ESSURE

FDA Adverse Event
Injury ·BAYER MEDICAL CARE INC.·Product code HHS·June 23, 2023

BIRMINGHAM HIP

FDA Adverse Event
Injury ·SMITH AND NEPHEW·Product code NXT·December 27, 2013

SELENIA DIMENSIONS

FDA Adverse Event
Malfunction ·HOLOGIC, INC.·Product code MUE·October 26, 2020

8100 ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·January 6, 2021

SYMPHONY

FDA Adverse Event
Malfunction ·SORIN CRM·Product code NVZ·October 7, 2016

TENDRIL DX

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL·Product code DTB·August 11, 2023

HAMILTON MEDICAL AG

FDA Adverse Event
Malfunction ·HAMILTON MEDICAL AG·Product code CBK·June 22, 2023