Lokomat 31002

GUDID 07640174660223

HOCOMA AG

Treadmill/elliptical gait rehabilitation system

• Primary Device ID: 07640174660223
• NIH Device Record Key: 4ea8bba2-da8c-4dbc-80b3-d531cdf1ae62
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lokomat
• Version Model Number: Nanos V1.2
• Catalog Number: 31002
• 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	07640174660223 [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: 2020-05-06
• Device Publish Date: 2016-08-22

On-Brand Devices [Lokomat]

• 07640174660254: Pro
• 07640174660247: Pro
• 07640174660223: Nanos V1.2
• 07640174660216: Nanos V1.2
• 07640174660209: Nanos V1.2
• 07640174660179: Pro
• 07640174660162: Pro
• 07640174660155: Pro
• 07640174660148: Pro
• 07640174660117: Pro
• 07640174660100: Pro
• 07640174660094: Pro
• 07640174660087: Pro
• 07640174660070: Pro
• 07640174660063: Pro
• 07640174660445: Pro 6.3 AD
• 07640174660438: Pro 6.3 Kombi
• 07640174660421: Pro 6.3 FD PE
• 07640174660414: Pro 6.3 FD AD
• 07640174660407: Pro 6.3 FD Kombi
• 07640174660490: Nanos 1.3
• 07640174660483: Pro 6.3 PE Motivation
• 07640174660476: Pro 6.3 AD Motivation
• 07640174660469: Pro 6.3 Kombi Motivation
• 07640174660452: Pro 6.3 PE