STRAUMANN MEMBRANEFLEX

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-07-21 for STRAUMANN MEMBRANEFLEX manufactured by Collagen Matrix, Inc..

Event Text Entries

[80921042] Collagen matrix has made multiple unsuccessful attempts to obtain additional product information (i. E. Lot number, expiration date, udi). Due to insufficient feedback a thorough assessment could not be completed.
Patient Sequence No: 1, Text Type: N, H10


[80921043] Clinician reported that the straumann membraneflex product resorbed within 2 weeks of being implanted. Typical resorption time for this membrane is 12-16 weeks.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2249852-2017-00005
MDR Report Key6734633
Date Received2017-07-21
Date of Report2017-02-21
Date Mfgr Received2016-08-01
Date Added to Maude2017-07-21
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactMS. GLORIA ZUCLICH
Manufacturer Street15 THORNTON ROAD
Manufacturer CityOAKLAND NJ 07436
Manufacturer CountryUS
Manufacturer Postal07436
Manufacturer Phone2014051477
Manufacturer G1COLLAGEN MATRIX, INC.
Manufacturer Street15 THORNTON ROAD
Manufacturer CityOAKLAND NJ 07436
Manufacturer CountryUS
Manufacturer Postal Code07436
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameSTRAUMANN MEMBRANEFLEX
Generic NameCOLLAGEN DENTAL MEMBRANE - CONFORMABLE PP
Product CodeNPL
Date Received2017-07-21
OperatorDENTIST
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCOLLAGEN MATRIX, INC.
Manufacturer Address15 THORNTON ROAD OAKLAND NJ 07436 US 07436


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-07-21

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