References:
1. CereLink bench test shows (2 stdev) of ±2.2 mmHg over 7 days and 3.8mmHg (4 stdev) over 7 days.
2. CereLink system IFUs

*The CereLink ICP Sensor is MR Conditional and the CereLink ICP Monitor is contraindicated for use in a Magnetic Resonance (MR) environment. See Instructions for Use for complete product information and specific MRI Safety Information. Read and understand the IFU in its entirety prior to performing a Magnetic Resonance Imaging Procedure on a patient with an implanted CereLink® ICP Sensor. Failure to adhere to the Conditions for Safe Use may result in serious injury to the patient.

826820 Indications for Use The ICP Monitor is intended for use as an interface between compatible strain gauge type pressure transducers and standard physiological pressure monitoring systems. The ICP Monitor is also intended for use as an independent pressure monitor for displaying the mean, systolic and diastolic values of a physiologic pressure waveform in the absence of an external patient monitor.

826850, 826851, 826852, 826854 Indications for Use • (826850, 826851, 826852) Use of the CereLink ICP Sensor Basic Kit and CereLink ICP Bolt Kit are indicated when direct intracranial pressure (ICP) monitoring is required. The kit is indicated for use in both subdural and intraparenchymal pressure monitoring applications only. • (826854) Use of the ICP Sensor Ventricular Catheter Kit is indicated when direct intraventricular pressure monitoring is required. The kit is indicated for use in ICP monitoring and cerebrospinal fluid (CSF) drainage applications.