Actiware CT 1103609

GUDID 00606959040366

Actiware Clinical Trial Software, English

Respironics, Inc.

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• Primary Device ID: 00606959040366
• NIH Device Record Key: b8289529-ebdc-4c77-b3a7-2d42744fbac3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Actiware CT
• Version Model Number: 6.0
• Catalog Number: 1103609
• Company DUNS: 080728314
• Company Name: Respironics, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• Phone: +1(724)744-2500
• Email: respironics.service@philips.com
• 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	00606959040366 [Primary]

FDA Product Code

• IKK: SYSTEM, ISOKINETIC TESTING AND EVALUATION

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: 2020-03-05
• Device Publish Date: 2016-09-15

Devices Manufactured by Respironics, Inc.

• 00606959051942 - Trilogy Evo: 2022-05-23 Trilogy Evo, USA
• 00606959417540 - DreamStation: 2022-01-10 Micro-Flexible Heated 12mm Tube
• 00606959060135 - Therapy Mask 3100: 2021-12-16 Medium Wide, Therapy Mask 3100 Silicone
• 00606959060098 - Therapy Mask 3100: 2021-11-04
• 00606959060104 - Therapy Mask 3100: 2021-11-04
• 00606959060128 - Therapy Mask 3100: 2021-11-04
• 00606959063082 - DreamStation 2: 2021-11-04
• 00606959063228 - DreamStation 2: 2021-11-04