Camino® PMIOMPM-1

GUDID M273PMIOMPM11

The Integra Camino PMIOMPM-1 cables are accessories for the Integra Camino Monitor range MPM-1, CAM01, CAM02 monitors and the Integra Licox PtO monitoring system. They are intended to be used to interface these monitors with 3rd Party patient bedside monitors. The device is a reusable product.

INTEGRA LIFESCIENCES (IRELAND) LIMITED

Electrical-only medical device connection cable, reusable

• Primary Device ID: M273PMIOMPM11
• NIH Device Record Key: e26cbdf2-672e-4163-bdc0-09b619089422
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Camino®
• Version Model Number: PMIOMPM-1
• Catalog Number: PMIOMPM-1
• Company DUNS: 989925396
• Company Name: INTEGRA LIFESCIENCES (IRELAND) LIMITED
• 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: true
• Serial Number: false
• 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)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com

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: +20% to +95%. Avoid excessive heat and humidity.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature: -20°C (-4°F) to +50°C (+122°F). Relative Humidity, non-condensing: +20% to +95%. Avoid excessive heat and humidity.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature: -20°C (-4°F) to +50°C (+122°F). Relative Humidity, non-condensing: +20% to +95%. Avoid excessive heat and humidity.

Device Identifiers

Device Issuing Agency	Device ID
GS1	10381780039570 [Primary]
HIBCC	M273PMIOMPM11 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121573

FDA Product Code

• GWM: DEVICE, MONITORING, INTRACRANIAL PRESSURE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2022-12-06
• Device Publish Date: 2016-12-29

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