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

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ROTA FLOW CENTRIFUGAL PUMP WITH BIOLINE COATING, MODELS BE-RF-32, BEQ-RF-32

FDA 510(k)
FDA Class 2 ·Cardiovascular

HLM TUBING SET W/BIOLINE COATING

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·March 25, 2016

R & D 4K RETIC

FDA 510(k)
FDA Class 2 ·Hematology

MODIFICATION TO CORLINK AUTOMATED ANASTOMOTIC DEVICE

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

SPECTRA WAVEWRITER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 7, 2021

HNM MEDICAL

FDA UDI
HNM STAINLESS, LLC.·00842962155776·PEEK, BASIC COUNTER RETRACTOR, DOUBLE HINGED ARMS

NON AC-POWERED PATIENT LIFT

FDA Adverse Event
Malfunction ·UNKNOWN·Product code FSA·April 26, 2013

NI

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 6, 2011

LINOX SD 65/18

FDA Adverse Event
Injury ·BIOTRONIK GMBH & CO.·Product code LWS·July 21, 2008

DURAMAX (TM) Hemodialysis Catheters, Stacked Tip 28 cm Straight Basic Kit, Catalog Number/REF 10302804, 510 (k) 080400, Sterile --- Manufactured in USA by AngioDynamics, Inc. 603 Queensbury Avenue, Queensbury, NY 12804

FDA Recall
Terminated ·Angiodynamics, Inc.·Product code MSD·January 8, 2010

DURAMAX (TM) Hemodialysis Catheters, Stacked Tip 40 cm Straight Basic Kit, Catalog Number/REF 10302807, 510 (k) 080400, Sterile --- Manufactured in USA by AngioDynamics, Inc. 603 Queensbury Avenue, Queensbury, NY 12804

FDA Recall
Terminated ·Angiodynamics, Inc.·Product code MSD·January 8, 2010

DURAMAX (TM) Hemodialysis Catheters, Stacked Tip 24 cm Straight Basic Kit, Catalog Number/REF 10302803, 510 (k) 080400, Sterile --- Manufactured in USA by AngioDynamics, Inc. 603 Queensbury Avenue, Queensbury, NY 12804

FDA Recall
Terminated ·Angiodynamics, Inc.·Product code MSD·January 8, 2010

DURAMAX (TM) Hemodialysis Catheters, Stacked Tip 22 cm Straight Basic Kit, Catalog Number/REF 10302802, 510 (k) 080400, Sterile --- Manufactured in USA by AngioDynamics, Inc. 603 Queensbury Avenue, Queensbury, NY 12804

FDA Recall
Terminated ·Angiodynamics, Inc.·Product code MSD·January 8, 2010

DURAMAX (TM) Hemodialysis Catheters, Stacked Tip 32 cm Straight Basic Kit, Catalog Number/REF 10302805, 510 (k) 080400, Sterile --- Manufactured in USA by AngioDynamics, Inc. 603 Queensbury Avenue, Queensbury, NY 12804

FDA Recall
Terminated ·Angiodynamics, Inc.·Product code MSD·January 8, 2010

DURAMAX (TM) Hemodialysis Catheters, Stacked Tip 36 cm Straight Basic Kit, Catalog Number/REF 10302806, 510 (k) 080400, Sterile --- Manufactured in USA by AngioDynamics, Inc. 603 Queensbury Avenue, Queensbury, NY 12804

FDA Recall
Terminated ·Angiodynamics, Inc.·Product code MSD·January 8, 2010

DURAMAX (TM) Hemodialysis Catheters, Stacked Tip 55 cm Straight Basic Kit, Catalog Number/REF 10302809, 510 (k) 080400, Sterile --- Manufactured in USA by AngioDynamics, Inc. 603 Queensbury Avenue, Queensbury, NY 12804

FDA Recall
Terminated ·Angiodynamics, Inc.·Product code MSD·January 8, 2010

DURAMAX (TM) Hemodialysis Catheters, Stack Tip 28 cm Pre-Curve Basic Kit, Catalog Number/REF 10302813, 510 (k) 080400, Sterile --- Manufactured in USA by AngioDynamics, Inc. 603 Queensbury Avenue, Queensbury, NY 12804

FDA Recall
Terminated ·Angiodynamics, Inc.·Product code MSD·January 8, 2010

DURAMAX (TM) Hemodialysis Catheters, Stack Tip 32 cm Pre-Curve Basic Kit, Catalog Number/REF 10302814, 510 (k) 080400, Sterile --- Manufactured in USA by AngioDynamics, Inc. 603 Queensbury Avenue, Queensbury, NY 12804

FDA Recall
Terminated ·Angiodynamics, Inc.·Product code MSD·January 8, 2010

DURAMAX (TM) Hemodialysis Catheters, Stack Tip 24 cm Pre-Curve Basic Kit, Catalog Number/REF 10302812, 510 (k) 080400, Sterile --- Manufactured in USA by AngioDynamics, Inc. 603 Queensbury Avenue, Queensbury, NY 12804

FDA Recall
Terminated ·Angiodynamics, Inc.·Product code MSD·January 8, 2010

DURAMAX (TM) Hemodialysis Catheters, Stack Tip 36 cm Pre-Curve Basic Kit, Catalog Number/REF 10302815, 510 (k) 080400, Sterile --- Manufactured in USA by AngioDynamics, Inc. 603 Queensbury Avenue, Queensbury, NY 12804

FDA Recall
Terminated ·Angiodynamics, Inc.·Product code MSD·January 8, 2010