SP 3.3MM RN, SLACTIVE 12MM, TIZR, NTP Adverse Event — Injury (MDR 0009613348-2020-24773)
SP 3.3MM RN, SLACTIVE 12MM, TIZR, NTP Adverse Event — Injury (MDR 0009613348-2020-24773) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SP 3.3MM RN, SLACTIVE 12MM, TIZR, NTP; Generic name: ENDOSSEOUS DENTAL IMPLANT; Manufacturer: INSTITUT STRAUMANN AG.
| Device | SP 3.3MM RN, SLACTIVE 12MM, TIZR, NTP |
|---|---|
| Generic name | ENDOSSEOUS DENTAL IMPLANT |
| Manufacturer | INSTITUT STRAUMANN AG |
| Report number | 0009613348-2020-24773 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | FOREIGN, HEALTH PROFESSIONAL |
| Narrative | THE BATCH NUMBER COULD NOT BE VERIFIED DUE TO INCOMPLETE OR MISSING INFORMATION AND / OR PRODUCT FROM THE CUSTOMER. OUR MANUFACTURING Q-SYSTEM ASSURES THAT PRODUCTION AND PROCESS CONTROLS ARE IN PLACE TO ENSURE THAT BATCHES CONFIRM TO THE APPLICABLE SPECIFICATIONS BEFORE THEY ARE DISTRIBUTED. THE FRACTURE OF A DENTAL IMPLANT IS A KNOWN LONG-TERM COMPLICATION OF ENDOSSEOUS DENTAL IMPLANTS. THE MANU |
| Source | openFDA MAUDE (device adverse events) |
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