| 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 | 
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | |
| Phone | 360-225-1212 | 
| CustomerService@lifeport.com | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00810050863001 [Primary] | 
| FPP | Stretcher, Hand-Carried | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2024-10-23 | 
| Device Publish Date | 2024-10-15 | 
| 00810050863278 - Patient Loading Utility System (PLUS) | 2025-09-19 PLUS, 66 IN STRUCTURE | 
| 00810050863285 - Patient Loading Utility System (PLUS) | 2025-09-19 PLUS, 66 IN STRUCTURE | 
| 00810050863261 - Patient Loading Utility System (PLUS) | 2025-09-16 ASSEMBLY, PLUS, 66 INCH | 
| 00810050863254 - Patient Loading Utility System (PLUS) | 2025-09-02 PLUS, 62 IN SPAR JUMPER STRUCTURE, KING AIR | 
| 00810050863247 - Patient Loading Utility System (PLUS) | 2025-08-28 ASSEMBLY - PLUS - MAJOR | 
| 00810050863230 - Patient Loading Utility System (PLUS) | 2025-08-22 ASSEMBLY - PLUS * PATIENT LOADING UTILITY SYSTEM | 
| 00810050863223 - Patient Loading Utility System (PLUS) | 2025-07-29 PLUS, 72 IN SPAR JUMPER STRUCTURE * KING AIR | 
| 00810050863216 - Patient Loading Utility System (PLUS) | 2025-07-28 PLUS, 66 IN STRUCTURE * PATIENT LOADING UTILITY SYSTEM |