24 results · 24ms · 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.

Maverick XL Percutaneous Transluminal Coronary Angioplasty Monorail Dilatation Cathete

FDA 510(k)
FDA Class 2 ·Cardiovascular

DermAssist®

FDA UDI
INNOVATIVE HEALTHCARE CORPORATION·20813172024583·Gloves, Exam, Vinyl, Non-Sterile, Powder-Free, ...

PILLING

FDA UDI
TELEFLEX INCORPORATED·24026704429961·

CARDINAL HEALTH

FDA UDI
Cardinal Health 200, LLC·10885425499199·SATIN IRIS SCISSORS

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702449167·ELVAREX 2/THIGH HIGH/SLANT-CLOSED TOE-ELEPHANTI...

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702616309·ELVAREX 2/KNEE HIGH/SLANT-CLOSED TOE-ELEPHANTIA...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197483896·WEINSTEIN Instrument Holder 63x200mm

PROPEP DELIVERY DEVICE

FDA 510(k)
FDA Class 2 ·General Hospital

20.1-INCH (51CM) COLOR LCD MONITOR CDL2010A (CCL204)

FDA 510(k)
FDA Class 2 ·Radiology

II Ring Retractor

FDA UDI
Automated Medical Products Corp.·00810118342639·Oval Ring Large 12” x 18.5” Titanium/Radiolucent

II Ring Retractor

FDA UDI
Automated Medical Products Corp.·00810118342646·Oval Ring Large 12” x 18.5”

OSTEONICS OMINIFIT 20 DEG. CUP INSERT

FDA Adverse Event
Injury ·HOWMEDICA INC.·Product code LWJ·June 13, 2000

SECURE-FIT HA ACETABULAR SHELL

FDA Adverse Event
Injury ·HOWMEDICA OSTEONICS·Product code MEH·June 13, 2000

T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code OZO·February 22, 2021

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 6, 2022

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 18, 2021

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·May 11, 2023

UNKNOWN DEPUY 40 DELTA HEAD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KXA·July 8, 2011

RELIANCE SYNERGY WASHER

FDA Adverse Event
STERIS CANADA CORPORATION·Product code MEC·June 11, 2013

MATTA PELVIC SYSTEM

FDA Adverse Event
Other ·Product code HRS·October 9, 2014