Adverse-event reports (MAUDE)
Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.
No adverse-event reports are linked to this device.
Recall history
No recalls linked.
Regulatory clearances
None linked.
Manufacturer compliance record
None in the loaded window.
Similar devices
- Drill Bit Cranial 2.1 mm / 4.0 mm Brainlab SE
- Drill Bit Cranial 2.1 mm / 2.5 mm Brainlab SE
- Drill Bit Cranial 2.4 mm / 2.5 mm Brainlab SE
- Drill Bit Cranial 3.4 mm / 3.8 mm Brainlab SE
- SEEG DRILL ADAPTOR 2.70MM MEDTECH
- 063377717 Philips Ultrasound LLC
- 10815212026987 Izi Medical Products, LLC
- 2430MCA Rayence Co., Ltd.
- 2430TCA Rayence Co., Ltd.
- 2D Perfusion Philips Medical Systems Nederland B.V.
- 2D Quantitative Analysis Philips Medical Systems Nederland B.V.
- 2D X-RAY LEKSELL FRAME REGST PLATES MEDTECH
Select up to two to place side-by-side with this device.