SOLIDITY UU041-01-1927

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-01-10 for SOLIDITY UU041-01-1927 manufactured by Ulrich Medical Usa.

MAUDE Entry Details

Report Number3005823819-2020-00001
MDR Report Key9577962
Report SourceHEALTH PROFESSIONAL
Date Received2020-01-10
Date of Report2020-01-10
Date of Event2019-12-11
Date Mfgr Received2019-12-11
Date Added to Maude2020-01-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
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
Manufacturer ContactMR. LOUIS MILOS
Manufacturer Street18221 EDISON AVE.
Manufacturer CityCHESTERFIELD MO 63005
Manufacturer CountryUS
Manufacturer Postal63005
Manufacturer Phone6365190268
Manufacturer G1ULRICH GMBH & CO. KG
Manufacturer StreetBUCHBRUNNENWEG 12 NA
Manufacturer CityULM, 89081
Manufacturer CountryGM
Manufacturer Postal Code89081
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSOLIDITY
Generic NameCENTER PIECE, TURQUOISE, 13MM, HEIGHT 19-27.5MM
Product CodeMQP
Date Received2020-01-10
Model NumberUU041-01-1927
Catalog NumberUU041-01-1927
Lot NumberNI
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerULRICH MEDICAL USA
Manufacturer Address18221 EDISON AVE. CHESTERFIELD MO 63005 US 63005


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-01-10

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