16 results · 53ms · Sources: EU EUDAMED, US FDA

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MDSS GmbH

Authorized representative
🇩🇪 Germany·388 Manufacturers·16562 Devices

JETSTREAM G3

FDA Adverse Event
Injury ·PATHWAY MED TECHNOLOGIES, INC.·Product code MCW·December 29, 2010

SIMON NITINOL VENA CAVA FILTER

FDA Adverse Event
Injury ·NITINOL MED TECHNOLOGIES, INC.·Product code DTK·January 10, 1995

BIOJECTOR B2000

FDA Adverse Event
Other ·BIOJECT MED TECHNOLOGIES, INC·Product code KZE·January 8, 2007

BIOJECTOR B2000

FDA Adverse Event
Other ·BIOJECT MED TECHNOLOGIES, INC·Product code KZE·January 9, 2007

CALYPSO BEACON TRANSPONDERS

FDA Adverse Event
Injury ·CALYPSO MED TECHNOLOGIES INC·Product code IYE·January 12, 2010

SUBCLAVIAN CATHETER

FDA Adverse Event
Malfunction ·NEOSTAR MED TECHNOLOGIES, INC.·Product code LFJ·August 28, 1995

SAFETRACE TX

FDA Adverse Event
Malfunction ·GLOBAL MED TECHNOLOGIES, INC./WYNDGATE TECHNOLOGIES DIV·Product code MMH·October 11, 2001

SAFETRACE

FDA Adverse Event
Malfunction ·WYNDGATE TECHNOLOGIES / DIV GLOBAL MED TECHNOLOGIES, INC.·Product code MMH·February 28, 2001

SAFETRACE

FDA Adverse Event
Malfunction ·WYNDGATE TECHNOLOGIES DIVISION/GLOBAL MED TECHNOLOGIES, INC.·Product code MMH·July 22, 1999

SAFETRACE

FDA Adverse Event
Malfunction ·WYNDGATE TECHNOLOGIES DIVISION GLOBAL MED TECHNOLOGIES, INC·Product code MMH·March 8, 1999

Acorn Regulatory Consultancy Services Ltd

Authorized representative
🇮🇪 Ireland·16 Manufacturers·10848 Devices

MedNet EC-REP C III GmbH

Authorized representative
🇩🇪 Germany·12 Manufacturers·77 Devices

MedNet EC-REP GmbH

Authorized representative
🇩🇪 Germany·464 Manufacturers·5263 Devices

Advena Services Limited

Importer
🇲🇹 Malta·40 Manufacturers

Emergo Europe B.V.

Authorized representative
🇳🇱 Netherlands·900 Manufacturers·22100 Devices