Integra® Camino®

GUDID M6101104HC1

Ventricular Bolt Monitoring Kit W/Cranial Access, Drain

INTEGRA PAIN MANAGEMENT

Manual cranial rotary handpiece, single-use

• Primary Device ID: M6101104HC1
• NIH Device Record Key: b2241bf4-2a7c-4fb5-9ffa-998484fcb7af
• Commercial Distribution Discontinuation: 2023-12-04
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Integra® Camino®
• Version Model Number: 1104HC
• Company DUNS: 030370299
• Company Name: INTEGRA PAIN MANAGEMENT
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: true
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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: +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
• 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
• 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
• 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
• 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
• 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 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)
• Special Storage Condition, Specify: Between 0 and 0 *Storage Environment Temperature: 20 C to 25 C (68 F to 77 F)

Device Identifiers

Device Issuing Agency	Device ID
GS1	10381780260370 [Primary]
HIBCC	M6101104HC1 [Secondary]

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2024-03-19
• Device Publish Date: 2016-09-16

On-Brand Devices [Integra® Camino®]

• M6101104HMC1: VENTRICULAR BOLT ICP MONITOR KIT W/CRANIAL ACCESS, DRAIN
• M6101104HC1: Ventricular Bolt Monitoring Kit W/Cranial Access, Drain
• M6101104BC1: Intracranial Pressure Monitoring Kit W/Cranial Access