NEUROVENT-PX

GUDID 04057834088410

RAUMEDIC AG

Intracerebral sensor catheter, short-term

• Primary Device ID: 04057834088410
• NIH Device Record Key: 9e6b5343-9ca2-430c-9123-e40ec995974e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NEUROVENT-PX
• Version Model Number: 091580-003
• Company DUNS: 332785323
• Company Name: RAUMEDIC AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +18886470070
• Email: neuromonitoring@raumedic.com
• Phone: +18886470070
• Email: neuromonitoring@raumedic.com
• Phone: +18886470070
• Email: neuromonitoring@raumedic.com
• Phone: +18886470070
• Email: neuromonitoring@raumedic.com
• Phone: +18886470070
• Email: neuromonitoring@raumedic.com
• Phone: +18886470070
• Email: neuromonitoring@raumedic.com
• Phone: +18886470070
• Email: neuromonitoring@raumedic.com
• Phone: +18886470070
• Email: neuromonitoring@raumedic.com
• Phone: +18886470070
• Email: neuromonitoring@raumedic.com
• Phone: +18886470070
• Email: neuromonitoring@raumedic.com
• Phone: +18886470070
• Email: neuromonitoring@raumedic.com
• Phone: +18886470070
• Email: neuromonitoring@raumedic.com
• Phone: +18886470070
• Email: neuromonitoring@raumedic.com

Device Dimensions

• Outer Diameter: 1.65 Millimeter
• Outer Diameter: 1.65 Millimeter
• Outer Diameter: 1.65 Millimeter
• Outer Diameter: 1.65 Millimeter
• Outer Diameter: 1.65 Millimeter
• Outer Diameter: 1.65 Millimeter
• Outer Diameter: 1.65 Millimeter
• Outer Diameter: 1.65 Millimeter
• Outer Diameter: 1.65 Millimeter
• Outer Diameter: 1.65 Millimeter
• Outer Diameter: 1.65 Millimeter
• Outer Diameter: 1.65 Millimeter
• Outer Diameter: 1.65 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04057834088410 [Primary]

FDA Product Code

• GWM: Device, monitoring, intracranial pressure

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-12-15
• Device Publish Date: 2025-12-05

Devices Manufactured by RAUMEDIC AG

• 04057834023541 - Tunneling KIT CH8: 2025-12-16
• 04057834090468 - Tunneling KIT CH12: 2025-12-16
• 04057834026115 - NEUROVENT-P: 2025-12-15
• 04057834082845 - NEUROVENT: 2025-12-15
• 04057834082876 - NEUROVENT-IFD-S: 2025-12-15
• 04057834082883 - NEUROVENT-IFD-R: 2025-12-15
• 04057834082906 - NEUROVENT-TEMP-IFD-S: 2025-12-15
• 04057834082913 - NEUROVENT-TEMP-IFD-R: 2025-12-15