LEVO LAE/L-XL/42/51

GUDID 07613045036762

Standup Wheelchair.

LEVO AG Wohlen

Push-rim manual wheelchair, non-bariatric

• Primary Device ID: 07613045036762
• NIH Device Record Key: 2da2c685-523d-4a5c-b056-e768b3a9e865
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LEVO
• Version Model Number: LAE
• Catalog Number: LAE/L-XL/42/51
• Company DUNS: 481093706
• Company Name: LEVO AG Wohlen
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613045036762 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K971873

FDA Product Code

• IPL: Wheelchair, Standup

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: 2025-09-17
• Device Publish Date: 2025-09-09

On-Brand Devices [LEVO]

• 07613045071503: Powered Standup Wheelchair.
• 07613045038940: Standup Wheelchair.
• 07613045036762: Standup Wheelchair.