SWORD Phoenix

GUDID 05600775530051

SWORD HEALTH, S.A.

Virtual-display rehabilitation system, non-supportive, home-use

• Primary Device ID: 05600775530051
• NIH Device Record Key: eda5b411-70ec-45b6-9167-6bf45617a244
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SWORD Phoenix
• Version Model Number: SWORD Phoenix 2.0 5MTs
• Company DUNS: 338007105
• Company Name: SWORD HEALTH, S.A.
• 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: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05600775530051 [Primary]

FDA Product Code

• ISD: Exerciser, Measuring

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: 2019-03-20
• Device Publish Date: 2019-03-12

On-Brand Devices [SWORD Phoenix]

• 05600775530051: SWORD Phoenix 2.0 5MTs
• 05600775530044: SWORD Phoenix 2.0 2MTs