AeroSled Turbo Sled (TS)

GUDID 00810050863001

AEROSLED TS

LIFEPORT, LLC

Ambulance stretcher, manual

• Primary Device ID: 00810050863001
• NIH Device Record Key: 58af2ab8-f853-4c6a-a383-9f75142def4d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AeroSled Turbo Sled (TS)
• Version Model Number: AS1-001-04
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810050863001 [Primary]

FDA Product Code

• FPP: Stretcher, Hand-Carried

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: 2024-10-23
• Device Publish Date: 2024-10-15

Devices Manufactured by LIFEPORT, LLC

• 00810050863162 - Powered Loading System (PLS) (Component): 2025-05-30 RAMP, ASSEMBLY * (PLS)
• 00810050863148 - Oxygen Bottle Assembly: 2025-05-23 ASSEMBLY, COMPOSITE BOTTLE, CGA 577 VALVE
• 00810050863155 - Medical Cabinet: 2025-05-23 ASSEMBLY, VARIABLE PUMP, MEDICAL CABINET
• 00810050863131 - Load Ramp: 2025-05-21 ASSEMBLY, LOAD RAMP, 58"
• 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