MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05 report with the FDA on 2012-07-05 for MEMBRAGEL 070.101 manufactured by Institut Straumann Ag.
[2870623]
Clinician reports that the implantation of a dental implant in site 12 took place on (b)(6)2011 with a simultaneous ridge augmentation procedure using bone ceramic and membrane membragel. The clinician reports that there was an infection approx in (b)(6) 2012. The gingiva was closed around the implant. There was a secondary infection of the membrane (membragel) and possibly bone ceramic. The membrane membragel was removed and it was re-sutured. The dental implants in sites 22/21/11 were saved.
Patient Sequence No: 1, Text Type: D, B5
[10000333]
Catalog #070. 101, membragel, package insert instructions for use state "treatment outcome is dependent on operative technique and patient response. As with any surgical procedure, infection is a risk. Use sterile intra-operative technique. Do not use at infected sites. " catalog #070. 101, membragel, package insert instructions for use state, "the following complications are common with the surgical intervention with barrier membranes and therefore may not be totally excluded: soft tissue dehiscence, hematoma, pain, inflammation, increased sensitivity and redness. "
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 1222315-2012-00008 |
| MDR Report Key | 2647873 |
| Report Source | 01,05 |
| Date Received | 2012-07-05 |
| Date of Report | 2012-07-05 |
| Date of Event | 2012-03-01 |
| Date Mfgr Received | 2012-06-06 |
| Device Manufacturer Date | 2010-11-01 |
| Date Added to Maude | 2012-07-11 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | DENTIST |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Manufacturer Contact | BERNIE MCDONALD |
| Manufacturer Street | 60 MINUTEMANN RD. |
| Manufacturer City | ANDOVER MA 01810 |
| Manufacturer Country | US |
| Manufacturer Postal | 01810 |
| Manufacturer Phone | 9787472514 |
| Manufacturer G1 | BIORA AB |
| Manufacturer Street | MEDEON SCIENCE PARK |
| Manufacturer City | MALMO |
| Manufacturer Country | SW |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | MEMBRAGEL |
| Generic Name | BARRIER MEMBRANE |
| Product Code | NPK |
| Date Received | 2012-07-05 |
| Catalog Number | 070.101 |
| Lot Number | AY470 |
| Device Expiration Date | 2012-11-30 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | INSTITUT STRAUMANN AG |
| Manufacturer Address | BASEL SZ |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 21 | 1. Other | 2012-07-05 |