OxyTip SpO2

GUDID 00840682103022

GE Healthcare Finland Oy

Pulse oximeter, line-powered

• Primary Device ID: 00840682103022
• NIH Device Record Key: 5f94c5ae-17bd-4a07-a082-086580c52749
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OxyTip SpO2
• Version Model Number: OXY-FMR-00
• Company DUNS: 401966697
• Company Name: GE Healthcare Finland Oy
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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)558-5120
• Email: xx@xx.xx

Operating and Storage Conditions

• Storage Environment Temperature: Between -40 Degrees Celsius and 60 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840682103022 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K062324

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: 2018-07-06
• Device Publish Date: 2016-06-16

On-Brand Devices [OxyTip SpO2]

• 00840682103077: OXY-WMR-00
• 00840682103022: OXY-FMR-00