Masimo Rainbow SET MCable

GUDID 04049098009744

DRAEGER MEDICAL SYSTEMS, INC.

Single-patient intensive/general healthcare physiologic monitoring system

• Primary Device ID: 04049098009744
• NIH Device Record Key: ea3b50df-fd87-4372-b50f-335c177004a4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Masimo Rainbow SET MCable
• Version Model Number: MS27900
• Company DUNS: 788289952
• Company Name: DRAEGER MEDICAL SYSTEMS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• 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

Customer Support Contacts

• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com
• Phone: +18004372437
• Email: info@draeger.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04049098009744 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K113798

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: 4
• Public Version Date: 2020-02-06
• Device Publish Date: 2015-10-24

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