Actiware 1143911

GUDID 00606959057753

Actiware, Software CD, US Gov.

Respironics, Inc.

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• Primary Device ID: 00606959057753
• NIH Device Record Key: 3e3efdc3-df3a-4c1c-bc84-2727e1c1a973
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Actiware
• Version Model Number: 6.0.11
• Catalog Number: 1143911
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00606959057753 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-05-22
• Device Publish Date: 2020-05-14

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