LIPOGEMS PROCESS DEVICE LGD 240 LG MK 240

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-27 for LIPOGEMS PROCESS DEVICE LGD 240 LG MK 240 manufactured by Lipogems International Spa.

MAUDE Entry Details

Report Number3006053983-2019-00001
MDR Report Key8937292
Date Received2019-08-27
Date of Report2019-05-16
Date of Event2018-05-11
Date Facility Aware2018-05-24
Date Added to Maude2019-08-27
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLIPOGEMS PROCESS DEVICE
Generic NameSPORT MEDICINE 240
Product CodeMUU
Date Received2019-08-27
Model NumberLGD 240
Catalog NumberLG MK 240
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerLIPOGEMS INTERNATIONAL SPA
Manufacturer AddressVIALE BIANCA MARIA, 24 MILAN, 20129 IT 20129


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-08-27

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