Genius 2 989803179381

GUDID 20884838028719

Philips Medical Systems

Single-patient intensive/general healthcare physiologic monitoring system

• Primary Device ID: 20884838028719
• NIH Device Record Key: a4b9659e-655d-4b08-aee5-c6753b029b80
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Genius 2
• Version Model Number: 989803179381
• Catalog Number: 989803179381
• Company DUNS: 078628040
• Company Name: Philips Medical Systems
• 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: true
• 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	10884838028712 [Unit of Use]
GS1	20884838028719 [Primary]

FDA Product Code

• MHX: MONITOR, PHYSIOLOGICAL, PATIENT(WITH 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: 3
• Public Version Date: 2020-02-06
• Device Publish Date: 2016-10-05

On-Brand Devices [Genius 2]

• 00884838030497: 989803180831
• 20884838028726: 989803179611
• 20884838028719: 989803179381