Nox RIP Belts Disposable X-Large 951052

GUDID 15694311110033

Nox Medical ehf.

Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph Polysomnograph

• Primary Device ID: 15694311110033
• NIH Device Record Key: bd04dd94-bb81-4b1d-82f0-e6acc1a73d51
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nox RIP Belts Disposable X-Large
• Version Model Number: NOX-RIPDXL2
• Catalog Number: 951052
• Company DUNS: 365741462
• Company Name: Nox Medical ehf.
• Device Count: 2
• 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: true
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 999-999-9999
• Email: support@noxmedical.com
• Phone: 999-999-9999
• Email: support@noxmedical.com
• Phone: 999-999-9999
• Email: support@noxmedical.com
• Phone: 999-999-9999
• Email: support@noxmedical.com
• Phone: 999-999-9999
• Email: support@noxmedical.com
• Phone: 999-999-9999
• Email: support@noxmedical.com
• Phone: 999-999-9999
• Email: support@noxmedical.com
• Phone: 999-999-9999
• Email: support@noxmedical.com
• Phone: 999-999-9999
• Email: support@noxmedical.com
• Phone: 999-999-9999
• Email: support@noxmedical.com
• Phone: 999-999-9999
• Email: support@noxmedical.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	15694311110033 [Primary]
GS1	15694311110989 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K151361

FDA Product Code

• MNR: Ventilatory Effort Recorder

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: 2016-09-16

On-Brand Devices [Nox RIP Belts Disposable X-Large]

• 15694311110194: NOX-RIPDXL14
• 15694311110033: NOX-RIPDXL2