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 2012-01-06 for MEMBRAGEL 070.101 manufactured by Institut Straumann Ag.

Event Text Entries

[2412778] Buccal bone augmentation only without implantation on (b)(6) 2011; regio 42 using bone ceramic and membragel. Perio cut / area closure stress-free. (b)(6) 2011 control visit: nice situation / no pain only strange feeling. (b)(6), 2011: still some pain / nice healing without swelling / some pain under pressure / no liquid secretion under pressure. (b)(6) 2011 control visit : gingiva area 43 some inflammation / a lot of plaque / cleaning / no pus / removal of little pieces (membragel? ). (b)(6) 2011 control visit: less pain / pus with and without pressure =>> removal. (b)(6) 2011 removal / emdogain regio 42 / a lot of pus / painful / extreme inflammation / strong bleeding / removal membragel and boneceramic / cleaning and rinsed with nacl. (b)(6) 2011 nice wound healing / suture removal / subsequent treatment ok.
Patient Sequence No: 1, Text Type: D, B5


[9594830] The batch record review has been carried out and confirms that the product was within specification.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1222315-2012-00003
MDR Report Key2406186
Report Source01,05
Date Received2012-01-06
Date of Report2012-01-06
Date of Event2011-10-12
Date Mfgr Received2011-12-08
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 NamePRODUCT CODE NPK - BARRIER MEMBRANE
Product CodeNPK
Date Received2012-01-06
Catalog Number070.101
Lot NumberZ5927
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 2012-01-06

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