MedWall

GUDID 00810050862103

COMPOSITE MEDWALL ASSEMBLY

LIFEPORT, LLC

Suction/irrigation system canister/bottle holder, single-use

• Primary Device ID: 00810050862103
• NIH Device Record Key: e6cfd79d-650e-488c-9baa-75eae14ab25a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MedWall
• Version Model Number: ST2-165-03-02
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810050862103 [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: 2022-08-03
• Device Publish Date: 2022-07-26

On-Brand Devices [MedWall]

• 00810050862066: COMPOSITE MEDWALL ASSEMBLY
• 00810050862103: COMPOSITE MEDWALL ASSEMBLY
• 00810050862424: COMPOSITE MEDWALL ASSEMBLY