CAMINO® FLEXEXT

GUDID 10381780040965

Camino Flex Extension Cable

NATUS MEDICAL INCORPORATED

Electrical-only medical device connection cable, reusable

• Primary Device ID: 10381780040965
• NIH Device Record Key: 8b73b4d5-3ecb-4c49-8441-15328cc0d5b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CAMINO®
• Version Model Number: FLEXEXT
• Catalog Number: FLEXEXT
• Company DUNS: 081325959
• Company Name: NATUS MEDICAL INCORPORATED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1-800-356-0007
• Email: Madison.Helpdesk@Natus.com
• Phone: 1-800-356-0007
• Email: Madison.Helpdesk@Natus.com

Device Dimensions

• Length: 8 Feet
• Length: 8 Feet

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Temperature: -20°C (-4°F) to +50°C (+122°F). Relative Humidity, non-condensing: +25% to +80%. Keep dry.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature: -20°C (-4°F) to +50°C (+122°F). Relative Humidity, non-condensing: +25% to +80%. Keep dry.

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382830048675 [Primary]
GS1	10381780040965 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121159

FDA Product Code

• GWM: Device, Monitoring, Intracranial Pressure

Sterilization

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

[10381780040965]

Moist Heat or Steam Sterilization

[10381780040965]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-07-08
• Device Publish Date: 2019-06-28

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• 10381780025511: POST CRANIOTOMY SUBDURAL PRESSURE MONITORING KIT
• 10381780023630: INTRACRANIAL PRESSURE-TEMPERATURE MONITORING KIT
• 10381780023623: OLM INTRACRANIAL PRESSURE MONITORING KIT
• 10381780039310: Intracranial Pressure and Temperature Monitor
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• 10381780040965: Camino Flex Extension Cable
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