Arch Assembly

GUDID 00810050863049

ASSEMBLY, ACCESSORY ARCH, TS SLED

LIFEPORT, LLC

Stretcher equipment holder

• Primary Device ID: 00810050863049
• NIH Device Record Key: d2358946-71a0-4f93-b066-3042204a77b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Arch Assembly
• Version Model Number: AR2-042-01
• Company DUNS: 556196210
• Company Name: LIFEPORT, 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: 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

Customer Support Contacts

• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com
• Phone: 360-225-1212
• Email: CustomerService@lifeport.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810050863049 [Primary]

FDA Product Code

• FOX: Stand, Infusion

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: 2024-12-26
• Device Publish Date: 2024-12-18

On-Brand Devices [Arch Assembly]

• 00810050860055: ACCESSORY ARCH ASSY
• 00810050860918: INSTALLATION, ACCESSORY ARCH
• 00810050861120: ASSEMBLY, ACCESSORY ARCH, TW SLED
• 00810050861113: ASSEMBLY, ACCESSORY ARCH, TS SLED
• 00810050861212: ASSEMBLY, ACCESSORY ARCH, AEROSLED TW * GROUND USE ONLY
• 00810050861205: ASSEMBLY, ARCH
• 00810050861199: ASSEMBLY, ARCH
• 00810050861182: ASSEMBLY, ARCH
• 00810050861557: ACCESSORY ARCH ASSY * PC-12
• 00810050861830: ACCESSORY ARCH ASSY
• 00810050862219: ACCESSORY ARCH ASSY
• 00810050863049: ASSEMBLY, ACCESSORY ARCH, TS SLED
• 00810050863070: ASSEMBLY, ACCESSORY ARCH