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

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DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM, MODEL DP-6900

FDA 510(k)
FDA Class 2 ·Radiology

AMC

FDA UDI
Advantage Medical Electronics, LLC·00849593063371·NIBP Y-Adapter,Philips(Agilent/HP)Hose(1 tube)t...

ATEC 0909-12

FDA UDI
Hologic, Inc.·15420045504837·9G (3.7MM) X 9CM, 12MM HANDPIECE

ALARMVIEW WIRELESS DATA NETWORK SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

SIMPLICITY EASY SOFT INFUSION SET

FDA 510(k)
FDA Class 2 ·General Hospital

ATEC 0909-12 Breast Biopsy and Excision System , 9 gauge, 9 centimeter handpiece (part number 0909-12), Rx, Sterile, Suros Surgical Systems, Inc. 6100 Technology Center DR. Indianapolis, IN 46278. The handpiece is inserted into the breast to the site of the area of interest. When the proper location/[position is achieved, the handpiece cuts and removes biopsy tissue.

FDA Recall
Terminated ·Hologic, Inc.·Product code KNW·February 1, 2010

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 2, 2013

OT VERIO PRO METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 16, 2014

LIFEVEST WCD 4000 SYSTEM

FDA Adverse Event
Death ·ZOLL LIFECOR CORPORATION·Product code MVK·May 4, 2011

Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is indicated for continuous subcutaneous infusion of insulin for the treatment of insulin-requiring diabetes.

FDA Enforcement
Class I ·Terminated·Animas Corporation·April 10, 2013

Stryker T2 Arthrodesis Nailing System. Manufacturer: Stryker Trauma GmbH, Professor-Kuntscher-Str. 1-5, 24232 Schonkirchen Germany. Distributed in the USA by Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The T2 Arthrodesis Nail is intended for the treatment of Knee Arthrodesis. The design of the T2 Arthrodesis Nail features a unique curvature which incorporates both femur ante curvature and knee valgus bend. Indications: Aseptic failed total knee arthro-plasty with or without bone loss; Failed external fixation, non unions and malunions; Periarticular fractures where repair is not possible; Pathologic fractures and tumor resections; Pseudoarthrosis and correct osteotomy; Ipsilateral femur fractures; and Open and closed femoral fractures.

FDA Enforcement
Class II ·Terminated·Stryker Howmedica Osteonics Corp.·July 25, 2012