| 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 |
| 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 | |
| Phone | 360-225-1212 |
| CustomerService@lifeport.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810050862448 [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 | 2023-06-13 |
| Device Publish Date | 2023-06-05 |
| 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) | 2024-10-23 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 |