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

• 00810050863032 - Patient Loading Utility System (PLUS): 2024-12-23 PLUS, 66 INCH LONG STRUCTURE
• 00810050863025 - MEDPAK: 2024-12-10 ASSEMBLY - MEDPAK * NO AIR, NO SUC - 1000W - 115VAC
• 00810050863018 - Clip Deck Assembly: 2024-11-05 CLIP DECK ASSEMBLY, 76.00 LONG, FOLDING * YELLOW
• 00810050863001 - AeroSled Turbo Sled (TS): 2024-10-23AEROSLED TS
• 00810050863001 - AeroSled Turbo Sled (TS): 2024-10-23 AEROSLED TS
• 00810050862998 - IV Pole: 2024-10-22 ASSEMBLY, IV POLE, 16G
• 00810050862981 - Clip Deck Assembly: 2024-10-08 CLIP DECK ASSEMBLY, 76.00 LONG, STRAIGHT * YELLOW
• 00810050862974 - Patient Loading Utility System (PLUS): 2024-09-19 ASSEMBLY - PLUS * 66", LB, 1000W, 230 VAC, AFROX, AIR, SUC, O2 DUAL, CGA
• 00810050862967 - Load Ramp: 2024-09-04 ASSEMBLY, LOAD RAMP, 70" * LOAD END 38.0, NO LEG