BLX Ø4.5 RB, SLACTIVE® 12MM, RXD Adverse Event — Injury (MDR 0009613348-2020-24703)
BLX Ø4.5 RB, SLACTIVE® 12MM, RXD Adverse Event — Injury (MDR 0009613348-2020-24703) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BLX Ø4.5 RB, SLACTIVE® 12MM, RXD; Generic name: ENDOSSEOUS DENTAL IMPLANT; Manufacturer: INSTITUT STRAUMANN AG.
| Device | BLX Ø4.5 RB, SLACTIVE® 12MM, RXD |
|---|---|
| Generic name | ENDOSSEOUS DENTAL IMPLANT |
| Manufacturer | INSTITUT STRAUMANN AG |
| Report number | 0009613348-2020-24703 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | FOREIGN, HEALTH PROFESSIONAL |
| Narrative | THE BATCH NUMBER COULD BE VERIFIED. 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 REMOVAL OF A DENTAL IMPLANT DURING SURGERY WITHOUT THE REPLACEMENT OF ANOTHER DENTAL IMPLANT IS A KNOWN INHERENT RISK OF THE PROCEDURE DUE TO EITHER LACK OF PRIMARY STABILITY OF THE |
| Source | openFDA MAUDE (device adverse events) |
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