| Primary Device ID | 00810050862592 |
| NIH Device Record Key | 8500fc34-8cdd-4568-941b-51f0206c0b57 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Adapter Installation |
| Version Model Number | ST2-814-01 |
| 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 |
| 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 | 00810050862592 [Primary] |
| FOX | Stand, Infusion |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-09-07 |
| Device Publish Date | 2023-08-30 |
| 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 |