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

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Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set

FDA 510(k)
FDA Class 2 ·Cardiovascular

Conventional Lead Apron .5mm Xtra Xtra Large 26 X 42

FDA UDI
Flow X Ray Corporation·00843696123949·Conventional Lead Apron .5mm XXL 26 X 42, Shimm...

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112830·BARRON VACUUM PUNCH 9.5MM

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112809·BARRON VACUUM PUNCH 8.75MM

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112960·CORNEAL TREPHINE BLADE8.75MM

ACUMATCH P-SERIES PRESS-FIT PLASMA, ACUMATCH P-SERIES PRESS-FIT, ACUMATCH L-SERIES PRESS-FIT

FDA 510(k)
FDA Class 2 ·Orthopedic

VERDICT-II

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

APTIMA

FDA Adverse Event
Malfunction ·Product code JJC·October 16, 2008

LIBERTY CYCLER SET, SINGEL CONN./EXT.DL

FDA Adverse Event
Malfunction ·REYNOSA MANUFACTURING·Product code FKX·June 28, 2013

SPRINT

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2011

ATTUNE PS FEM LT SZ 7 CEM

FDA Adverse Event
Injury ·DEPUY IRELAND - 9616671·Product code OIY·May 25, 2021

ATTUNE PS RP INSRT SZ7 6MM

FDA Adverse Event
Injury ·DEPUY IRELAND - 9616671·Product code NJL·May 25, 2021

ATTUNE RP TIB BASE SZ 8 CEM

FDA Adverse Event
Injury ·DEPUY IRELAND - 9616671·Product code NJL·May 25, 2021

ATTUNE MEDIAL DOME PAT 41MM

FDA Adverse Event
Injury ·DEPUY IRELAND - 9616671·Product code OIY·May 25, 2021

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·June 30, 2021

MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAN·August 25, 2021

VCL+ VIO 36IN 2-0 S/A CT-1

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·September 23, 2021

GYNECARE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTO·August 25, 2021

HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP

FDA Adverse Event
Injury ·HEARTWARE, INC.·Product code DSQ·January 28, 2022