Bactiseal Catheter Safety Registry Study

Exclusion Criteria

• •1. A subject didn't have an indication suitable to use the catheter.
• •2. A subject was known to be allergic to a component or ingredient of the catheter to be implanted, including silicone catheter, rifampicin, and clindamycin.
• •3. According to the comprehensive judgment of an investigator, a subject had an infection of the implant site when the shunt is implanted, such as ventriculitis, meningitis, peritonitis, and local implant skin infection.
• •4. A subject was simultaneously implanted with another shunt catheter different from Bactiseal Catheter.
• •5. A subject had a contraindication of the shunt operation.
• •6. A subject had uncorrected coagulopathy or any bleeding disorder.