Erigo 29672

GUDID 07640174660056

HOCOMA AG

Physical therapy table, line-powered

• Primary Device ID: 07640174660056
• NIH Device Record Key: f3f7235a-a6c6-4a1d-970d-fb9a06b31ab8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Erigo
• Version Model Number: Basic
• Catalog Number: 29672
• 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	07640174660056 [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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-22

On-Brand Devices [Erigo]

• 07640174660131: Basic
• 07640174660056: Basic
• 07640174660032: Basic
• 07629999033894: Pro