| Primary Device ID | 00810050862035 |
| NIH Device Record Key | adf99f0a-5ef1-48dd-a68a-df48da5e8322 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Powered Loading System (PLS) (Wheelchair, PM) |
| Version Model Number | 21-10081-01 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810050862035 [Primary] |
| PCE | Permanently Mounted Wheelchair Platform Lift |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-07-01 |
| Device Publish Date | 2022-06-23 |
| 00810050862035 | INSTALLATION, RAIL ASSEMBLY, GLOBAL PLS * (WHEELCHAIR, PM) |
| 00810050862172 | INSTALLATION, POWER LOADING SYSTEM, FALCON * PLS, WHEELCHAIR |
| 00810050862288 | AIR STAIR ASSY NO MOD G 3-5 * (PLS) (WHEELCHAIR) |