35 results · 31ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970010·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970027·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172974018·UniTip High Resolution Catheter 10F

AUTOCLAVABLE CAMER HEAD MODEL OTV-Y0017

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

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112526·BARRON VACUUM TREPHINE 8.25MM

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523166121·MIS Acetabular Reamer, 59mm

8100/8500 VITAL SIGNS MONITOR

FDA 510(k)
FDA Class 2 ·Cardiovascular

AMT SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172973257·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172973677·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172973301·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970041·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970065·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970034·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970058·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172973004·

V200 / ESPRIT

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 16, 2021

RESPIRONICS

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 28, 2021

RESPIRONICS

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·May 19, 2021

N-FORCE FC SCREW 4.0X45MM

FDA Adverse Event
Injury ·INNOVISION, INC.·Product code HWC·August 8, 2019