Valedo 31081

GUDID 07640174660261

HOCOMA AG

Virtual-display rehabilitation system, non-supportive, clinical

• Primary Device ID: 07640174660261
• NIH Device Record Key: 41ea4fe4-c4c7-4c33-8ec1-44fd5d15c70b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Valedo
• Version Model Number: Motion
• Catalog Number: 31081
• 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640174660261 [Primary]

FDA Product Code

• KQX: Goniometer, Ac-Powered

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: 2016-08-24

On-Brand Devices [Valedo]

• 07640174660261: Motion
• 07629999023710: Valedo