Hand Pad Horn Type

GUDID 04064406066820

Otto Bock Mobility Solutions GmbH

Wheelchair armrest Wheelchair armrest Wheelchair armrest Wheelchair armrest Wheelchair armrest Wheelchair armrest Wheelchair armrest Wheelchair armrest Wheelchair armrest Wheelchair armrest Wheelchair armrest Wheelchair armrest Wheelchair armrest Wheelchair armrest Wheelchair armrest Wheelchair armrest Wheelchair armrest

• Primary Device ID: 04064406066820
• NIH Device Record Key: 60483e62-b46e-4333-8571-776d9d11ea72
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hand Pad Horn Type
• Version Model Number: 436P3=R2-7
• Company DUNS: 341148586
• Company Name: Otto Bock Mobility Solutions 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: false
• 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	04064406066820 [Primary]

FDA Product Code

• KNO: Accessories, Wheelchair

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: 2023-12-27
• Device Publish Date: 2023-12-19

On-Brand Devices [Hand Pad Horn Type]

• 04064406066820: 436P3=R2-7
• 04064406066813: 436P3=R1-7
• 04064406066806: 436P3=L2-7
• 04064406066790: 436P3=L1-7