CNAP SENSOR CUFF, LARGE

GUDID 04049098005692

DRAEGER MEDICAL SYSTEMS, INC.

Patient monitoring system module, blood pressure, noninvasive

• Primary Device ID: 04049098005692
• NIH Device Record Key: 72b0b692-1614-4e47-b2e4-20fd8adf22e9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CNAP SENSOR CUFF, LARGE
• Version Model Number: MS15896
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04049098005692 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102968

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive

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: 2015-11-02

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