| Primary Device ID | 00810050863360 |
| NIH Device Record Key | 165e3a57-f87b-4499-abad-d56d3e5f2d8b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Transition Deck |
| Version Model Number | MD1-013-01-MOD |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810050863360 [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 | 2026-02-04 |
| Device Publish Date | 2026-01-27 |
| 00810050861618 | ASSEMBLY, TRANSITION DECK, 4G LOCKS |
| 00810050863360 | ASSEMBLY, TRANSITION DECK, 4G LOCKS |