Manovo 29568

GUDID 07640174660377

HOCOMA AG

Virtual-display rehabilitation system, powered-support, upper-limb

• Primary Device ID: 07640174660377
• NIH Device Record Key: fdfa73b7-9534-4e1f-8778-7be40d81504b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Manovo
• Version Model Number: Spring
• Catalog Number: 29568
• 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	07640174660377 [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: 2023-10-19
• Device Publish Date: 2023-10-11

Devices Manufactured by HOCOMA AG

• 07640174660353 - Armeo: 2023-10-19
• 07640174660377 - Manovo: 2023-10-19
• 07640174660377 - Manovo: 2023-10-19
• 07640174660391 - Armeo: 2023-10-19
• 07640174660452 - Lokomat: 2023-03-31
• 07640174660469 - Lokomat: 2023-03-31
• 07640174660476 - Lokomat: 2023-03-31
• 07640174660483 - Lokomat: 2023-03-31
• 07640174660490 - Lokomat: 2023-03-31