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

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REICHERT CT200 CONTACT TONOMETER

FDA 510(k)
FDA Class 2 ·Ophthalmic

Varisoft™

FDA UDI
Unomedical A/S·05705244014817·Single use infusion set for subcutaneous infusi...

ADVANCE®

FDA UDI
Microport Orthopedics Inc.·M684K00012881·

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·00304040073216·Carbide Bur FG 2

CONMED

FDA UDI
Conmed Corporation·10653405050810·American Dilator, Reusable, 18F

Visby Medical Power Adapter

FDA UDI
Visby Medical, Inc.·00810031720033·Visby Medical Power Adapter.

MEDELA THOPAZ, MODEL 200 0288

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

LIFEPAK 15 monitor/defibrillator

FDA UDI
PHYSIO-CONTROL, INC.·00883873870235·LP15 ACCRY SHIPKIT,AHA,S

ENTEC CONTROLLER, ENTEC PATIENT CABLE, FOOTSWITCH, POWERCORD, PLASMA WAND

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

HSV-1 & HSV-2 DIFFERENTIATION IMMUNOBLOT IGG, MODEL IB0900G

FDA 510(k)
FDA Class 2 ·Microbiology

EVOLUTION MP CS INSERT SIZE 7 STANDARD 10MM LEFT

FDA Adverse Event
Injury ·MICROPORT ORTHOPEDICS INC.·Product code HRY·March 16, 2020

TORNIER AFFINITI SHOULDER SURGICAL TRAY

FDA Adverse Event
Malfunction ·TORNIER, INC·Product code LRP·June 7, 2009

EVOLUTION MP CS INSERT SIZE 8 STANDARD 12MM LEFT

FDA Adverse Event
Malfunction ·MICROPORT ORTHOPEDICS INC.·Product code HRY·April 13, 2020

LIBERTÉ?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·March 12, 2013

SECURE II MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·February 18, 2011

AED PLUS

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 14, 2008

PROWLER SELECT PLUS 150/5CM

FDA Adverse Event
Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRA·May 23, 2023

ADVANCE® ONLAY ALL-POLY PATELLA 32MM TRI-PEG

FDA Adverse Event
Injury ·MICROPORT ORTHOPEDICS INC.·Product code JWH·November 1, 2022

EVOLUTION® NITRX? TIB KEELED

FDA Adverse Event
Injury ·MICROPORT ORTHOPEDICS INC.·Product code JWH·November 7, 2022

EVOLUTION® NITRX? TIB KEELED

FDA Adverse Event
Injury ·MICROPORT ORTHOPEDICS INC.·Product code JWH·November 7, 2022