zRIP DuraBelt 1076329

GUDID 00606959010369

zRIP Durabelt Kit, Adult

Respironics, Inc.

Polysomnograph

• Primary Device ID: 00606959010369
• NIH Device Record Key: 59f80022-411f-4655-a229-00a8946f2d72
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: zRIP DuraBelt
• Version Model Number: ZRIP DURABELT
• Catalog Number: 1076329
• 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: true
• 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

Operating and Storage Conditions

• Storage Environment Humidity: Between 15 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 15 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 15 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
• Storage Environment Temperature: Between -4 Degrees Fahrenheit and 140 Degrees Fahrenheit
• Storage Environment Temperature: Between -20 Degrees Celsius and 60 Degrees Celsius
• Storage Environment Humidity: Between 15 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	00606959010369 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K013905

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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-18

On-Brand Devices [zRIP DuraBelt]

• 00606959010550: zRIP Durabelt, Belt Only, Pediatric
• 00606959010543: zRIP Durabelt, Adult, Large
• 00606959010499: zRIP Durabelt Kit, Pediatric, QDC
• 00606959010482: zRIP Durabelt Kit, Adult, QDC
• 00606959010437: zRIP Durabelt Kit, Pediatric, A5
• 00606959010420: zRIP Durabelt Kit, Adult, A5
• 00606959010413: Alice 6 zRIP Pediatric Kit
• 00606959010406: zRIP Durabelt Kit, Adult, PDx
• 00606959010390: zRIP Durabelt Sum RT Kit, Pediatric
• 00606959010383: zRIP Durabelt Sum RT Kit, Adult
• 00606959010376: zRIP Durabelt Kit, Pediatric
• 00606959010369: zRIP Durabelt Kit, Adult
• 00606959004818: zRIP DuraBelt Kit, Adult, Alice 6
• 00606959004696: zRIP Durabelt, Adult