DIERS leg axis lateral

GUDID 04260242060125

DIERS International GmbH

Biomechanical function analysis system, motion-tracking Biomechanical function analysis system, motion-tracking Biomechanical function analysis system, motion-tracking Biomechanical function analysis system, motion-tracking Biomechanical function analysis system, motion-tracking Biomechanical function analysis system, motion-tracking Biomechanical function analysis system, motion-tracking Biomechanical function analysis system, motion-tracking Biomechanical function analysis system, motion-tracking Biomechanical function analysis system, motion-tracking Biomechanical function analysis system, motion-tracking Biomechanical function analysis system, motion-tracking

• Primary Device ID: 04260242060125
• NIH Device Record Key: b421749f-c79c-4cbc-a993-c43c007fc0fd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DIERS leg axis lateral
• Version Model Number: n/a
• Company DUNS: 499189983
• Company Name: DIERS International GmbH
• 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: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260242060125 [Primary]

FDA Product Code

• KQX: Goniometer, Ac-Powered

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: 2023-06-12
• Device Publish Date: 2023-06-02

On-Brand Devices [DIERS leg axis lateral]

• 04260242060170: HP
• 04260242060125: n/a