MEMBRAGEL 070.101

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2012-01-06 for MEMBRAGEL 070.101 manufactured by Institut Straumann Ag.

Event Text Entries

[16580903] Clinician reports a problem with membragel. Clinician told straumann employee that she used membragel and about one week later, the pt presented with an infection and what appeared to be pus. Root cause unk. Clinician is not blaming membragel and will follow up with pt in about a week.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1222315-2012-00004
MDR Report Key2406185
Report Source05
Date Received2012-01-06
Date of Report2012-01-06
Date Mfgr Received2011-12-09
Date Added to Maude2012-01-11
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationDENTIST
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactBERNIE MCDONALD
Manufacturer Street60 MINUTEMAN RD.
Manufacturer CityANDOVER MA 01810
Manufacturer CountryUS
Manufacturer Postal01810
Manufacturer Phone9787472514
Manufacturer G1BIORA AB
Manufacturer StreetMEDEON SCIENCE PARK
Manufacturer CityMALMO
Manufacturer CountrySW
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMEMBRAGEL
Generic NamePROD CODE NPK - BARRIER MEMBRANE
Product CodeNPK
Date Received2012-01-06
Catalog Number070.101
Lot NumberAG318
Device Expiration Date2012-08-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerINSTITUT STRAUMANN AG
Manufacturer AddressBASEL SZ


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2012-01-06

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