MAQUET EDI CATHETER REF 6685775, 6/49 FR/CM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-06-25 for MAQUET EDI CATHETER REF 6685775, 6/49 FR/CM manufactured by Maquet Medical Systems, Usa.

MAUDE Entry Details

Report NumberMW5087601
MDR Report Key8735018
Date Received2019-06-25
Date of Report2019-06-21
Date of Event2019-06-20
Date Added to Maude2019-06-26
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag0
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameMAQUET EDI CATHETER REF 6685775, 6/49 FR/CM
Generic NameGASTROINTESTINAL, TUBES WITH ENTERAL SPECIFIC CONNECTORS
Product CodePIF
Date Received2019-06-25
Returned To Mfg2019-06-20
Model NumberMAQUET EDI CATHETER REF 6685775
Catalog NumberMAQUET EDI CATHETER REF 668577
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerMAQUET MEDICAL SYSTEMS, USA
Manufacturer AddressUS


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-06-25

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