LASS LP1001

GUDID 00853714008059

LASS Base Board

RADUX DEVICES, LLC

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• Primary Device ID: 00853714008059
• NIH Device Record Key: cc808cdd-5a53-404a-98af-1965b58e43b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LASS
• Version Model Number: LP1001
• Catalog Number: LP1001
• Company DUNS: 079668796
• Company Name: RADUX DEVICES, LLC
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com
• Phone: 800-935-3137
• Email: customerservice@raduxdevices.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00853714008059 [Primary]

FDA Product Code

• CCX: Support, Patient Position

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: 2024-02-08
• Device Publish Date: 2024-01-31

On-Brand Devices [LASS]

• 00853714008073: LASS Small Foam
• 00853714008066: LASS Large Foam
• 00853714008059: LASS Base Board
• 00853714008042: LASS Arm Board