Ferno #9 Conversion

GUDID 00810050862448

TS-FERNO #9 CONVERSION ASSEMBLY * RED

LIFEPORT, LLC

Ambulance stretcher docking device

• 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

• 00810050863094 - Patient Loading Utility System (PLUS): 2025-04-29 ASSEMBLY - PLUS
• 00810050863100 - Patient Loading Utility System (PLUS): 2025-04-29 ASSEMBLY - PLUS - MAJOR
• 00810050863117 - Load Ramp: 2025-04-29 cASSEMBLY, LOAD RAMP, 70"
• 00810050863124 - Arch Assembly: 2025-04-29 ASSEMBLY, ACCESSORY ARCH, TS SLED, KA
• 00810050863063 - Medical Cabinet: 2025-02-05 CABINET ASSEMBLY, 18' LOAD BAY
• 00810050863070 - Arch Assembly: 2025-02-05 ASSEMBLY, ACCESSORY ARCH
• 00810050863087 - Load Ramp: 2025-02-05 ASSEMBLY, LOAD RAMP, 70"
• 00810050863056 - Clip Deck Assembly: 2025-02-04 CLIP DECK ASSEMBLY, 68.00 LONG, FOLDING * RED