Infinium Medical

GUDID 00820870070345

INFINIUM MEDICAL, INC.

Single-patient physiologic monitoring system Single-patient physiologic monitoring system

• Primary Device ID: 00820870070345
• NIH Device Record Key: d1a5f3b3-872f-488a-9402-f4a7d4369058
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Infinium Medical
• Version Model Number: OMNI III
• Company DUNS: 037504771
• Company Name: INFINIUM MEDICAL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does n
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00820870070345 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-03-06

On-Brand Devices [Infinium Medical]

• 00820870070345: OMNI III
• 00852087007058: OMNI
• 00852087007041: CLEO
• 00852087007027: OMNI II
• 00852087007010: OMNI Express
• 00852087007003: OMNI K
• 00852087007034: OMNI III
• 00852087007522: OMNI II K