Armeo 30806

GUDID 07640174660193

HOCOMA AG

Virtual-display rehabilitation system, powered-support

• Primary Device ID: 07640174660193
• NIH Device Record Key: b5268611-cccf-4f2b-975a-d1e3598e8cee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Armeo
• Version Model Number: Power
• Catalog Number: 30806
• 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	07640174660193 [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: 2018-06-26
• Device Publish Date: 2016-08-22

On-Brand Devices [Armeo]

• 07640174660285: ArmeoSenso
• 07640174660193: Power
• 07640174660186: Power
• 07640174660025: Boom
• 07640174660018: Spring Pediatric
• 07640174660001: Spring
• 07640174660391: Support Harness
• 07640174660353: Spring Pro