KIT,SAMPLE,AGENTS,3160 989803152661

GUDID 00884838107304

INVIVO CORPORATION

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• Primary Device ID: 00884838107304
• NIH Device Record Key: b4ad0392-0d06-4191-a9fc-3cfb965dc874
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KIT,SAMPLE,AGENTS,3160
• Version Model Number: 989803152661
• Catalog Number: 989803152661
• Company DUNS: 013649151
• Company Name: INVIVO CORPORATION
• 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838107304 [Primary]

FDA Product Code

• MWI: Monitor, physiological, patient (without arrhythmia detection or alarms)

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-07-08
• Device Publish Date: 2021-06-30

On-Brand Devices [KIT,SAMPLE,AGENTS,3160]

• 00884838045088: 989803152661
• 00884838107304: 989803152661