Valmax

GUDID 00860011289289

Supply Line Medical

Manual traction wheelchair

• Primary Device ID: 00860011289289
• NIH Device Record Key: 81dc5b4c-702f-4dc7-8225-c139358a84d0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Valmax
• Version Model Number: DME.011
• Company DUNS: 117011784
• Company Name: Supply Line Medical
• Device Count: 1
• DM Exempt: false
• 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: false
• Manufacturing Date: false
• 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	00860011289289 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112816

FDA Product Code

• IOR: Wheelchair, Mechanical

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: 2025-03-03
• Device Publish Date: 2025-02-21

On-Brand Devices [Valmax]

• 00860011289241: PPE1117XL
• 00860011289234: PPE1117S
• 00860011289227: PPE1117M
• 00860011289210: PPE1117L
• 06974231101321: DME.132
• 06974231101307: DME.130
• 06974231101291: DME.011
• 06974231101284: DME.015
• 06974231101277: DME.003
• 06974231101260: DME.004
• 00860013569822: DME.076
• 00860013569815: DME.019
• 00860013569808: DME.018
• 00860011289296: DME.130
• 00860011289289: DME.011
• 00860011289272: DME.015
• 00860011289265: DME.004
• 00860011289258: DME.003
• 00199284755567: DME.132
• 00860013569839: DME.132
• 00860013569891: DME.016
• 00860013569884: VK3E18
• 00860013569877: VK2E20
• 00860013569846: V16K2ADAELR
• 00860014621802: DME.014