MEMBRAGEL 070.101

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05 report with the FDA on 2011-08-22 for MEMBRAGEL 070.101 manufactured by Institut Straumann Ag.

Event Text Entries

[18121765] On (b)(6) 2011 surgery with use of membragel, 0. 8 ml article number 070. 101, batch z5930 and straumann bone ceramic, 0. 4-0. 7mm, 0. 25g, article 070. 203, batch y8040. Clinician reports on (b)(6) 2011 after using membragel and bone ceramic the patient had loss of membragel and fistula discovered on (b)(6) 2011. Provisional bridge was inserted on (b)(6) 2011.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1222315-2011-00032
MDR Report Key2227040
Report Source01,05
Date Received2011-08-22
Date of Report2011-08-22
Date of Event2011-07-29
Date Mfgr Received2011-07-22
Date Added to Maude2011-09-02
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 NameBARRIER MEMBRANE
Product CodeNPK
Date Received2011-08-22
Catalog Number070.101
Lot NumberZ5930
Device Expiration Date2012-05-31
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 2011-08-22

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