Ferno #9 Conversion

GUDID 00810050862448

TS-FERNO #9 CONVERSION ASSEMBLY * RED

LIFEPORT, LLC

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• Primary Device ID: 00810050862448
• NIH Device Record Key: c4e35969-e8bc-4321-96f6-6cb537991755
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ferno #9 Conversion
• Version Model Number: 100-4206-02-01
• 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	00810050862448 [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: 2023-06-13
• Device Publish Date: 2023-06-05

Devices Manufactured by LIFEPORT, LLC

• 00810050862851 - Machined Medical Litter (AeroSled MA): 2024-04-19 AEROSLED, MACHINED, TD WITH CG PLACARD
• 00810050862844 - Patient Loading Utility System (PLUS): 2024-04-04 PLUS ASSEMBLY, KING AIR, 44.00 LONG
• 00810050862837 - Stanchion Litter System (SLS): 2024-04-02 MODEL 15-0026 STANCHION LITTER SYSTEM (SLS)
• 00810050862820 - STANCHION LITTER SYSTEM: 2024-04-01 MODEL 15-0026 STANCHION LITTER SYSTEM (SLS)
• 00810050862813 - MedDeck: 2024-03-19 TOP DECK ASSEMBLY - DHC-8
• 00810050862806 - AeroSled Transport Deck (TD): 2024-03-12 ASSEMBLY, AEROSLED TD, LOW G, WITH ROLLING FEET * RED
• 00810050862769 - Triple Litter Stacking System (TLSS): 2024-02-23 MODEL 15-0026 TRIPLE LITTER STACKING SYSTEM (TLSS)
• 00810050862776 - Equipment Mount: 2024-02-23 INSTALLATION, MOUNT, UTILITY