| Primary Device ID | 00810050861212 |
| NIH Device Record Key | d2178047-08b3-41cb-b292-a6d68de584e7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Arch Assembly |
| Version Model Number | AR2-034-01 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810050861212 [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 | 2021-06-04 |
| Device Publish Date | 2021-05-27 |
| 00810050860055 | ACCESSORY ARCH ASSY |
| 00810050860918 | INSTALLATION, ACCESSORY ARCH |
| 00810050861120 | ASSEMBLY, ACCESSORY ARCH, TW SLED |
| 00810050861113 | ASSEMBLY, ACCESSORY ARCH, TS SLED |
| 00810050861212 | ASSEMBLY, ACCESSORY ARCH, AEROSLED TW * GROUND USE ONLY |
| 00810050861205 | ASSEMBLY, ARCH |
| 00810050861199 | ASSEMBLY, ARCH |
| 00810050861182 | ASSEMBLY, ARCH |
| 00810050861557 | ACCESSORY ARCH ASSY * PC-12 |
| 00810050861830 | ACCESSORY ARCH ASSY |
| 00810050862219 | ACCESSORY ARCH ASSY |