| Primary Device ID | 00810050862653 | 
| NIH Device Record Key | fe4fd218-111a-40a5-81d3-07b4ca0dff1e | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Side Arch | 
| Version Model Number | 0202-0701-01-01-05 | 
| 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 | true | 
| 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 | 00810050862653 [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 | 2023-11-01 | 
| Device Publish Date | 2023-10-24 | 
| 00810050861380 | INSTALLATION, SIDE ARCH, PIAGGIO P180 | 
| 00810050862653 | INSTALLATION - SIDE ARCH |