Valedo 30811

GUDID 07629999023710

HOCOMA AG

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

• Primary Device ID: 07629999023710
• NIH Device Record Key: 2f53c147-ecc6-4692-bd69-7d9f2b5e7acd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Valedo
• Version Model Number: Valedo
• Catalog Number: 30811
• Company DUNS: 487876203
• Company Name: HOCOMA AG
• 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: 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	07629999023710 [Primary]

FDA Product Code

• ION: Exerciser, Non-Measuring

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-23

On-Brand Devices [Valedo]

• 07640174660261: Motion
• 07629999023710: Valedo