NightBalance RPL2CHST01

GUDID 00606959058743

Philips NightBalance - Replacement Chest Strap

Respironics, Inc.

Behavioural therapy electrical stimulation system Behavioural therapy electrical stimulation system

• Primary Device ID: 00606959058743
• NIH Device Record Key: 331467a5-43e9-4620-b335-bd2481294026
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NightBalance
• Version Model Number: 00
• Catalog Number: RPL2CHST01
• Company DUNS: 080728314
• Company Name: Respironics, Inc.
• 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: false
• Lot Batch: true
• Serial Number: false
• 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(724)744-2500
• Email: RESPIRONICS.SERVICE@PHILIPS.COM
• Phone: +1(724)744-2500
• Email: RESPIRONICS.SERVICE@PHILIPS.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00606959058743 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K180608

FDA Product Code

• MYB: Pillow, cervical (for mild sleep apnea)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-03-05
• Device Publish Date: 2020-02-26

On-Brand Devices [NightBalance]

• 00606959058743: Philips NightBalance - Replacement Chest Strap
• 30606959059598: Philips NightBalance, Canada
• 30606959059581: Philips NightBalance, Iberia
• 30606959057518: Philips NightBalance, Denmark
• 30606959054630: NightBalance Sleep Position Trainer System, Germany
• 30606959054616: NightBalance Sleep Position Trainer System, UK