| Primary Device ID | 01002022117307 |
| NIH Device Record Key | db7c6517-0afe-4526-bb82-7089bfe5b5ba |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Advance Plus Universal IV Administration Set |
| Version Model Number | 1730WY |
| Catalog Number | 1730WY |
| Company DUNS | 180572216 |
| Company Name | Exel International |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00020221117301 [Primary] |
| GS1 | 01002022117307 [Package] Contains: 00020221117301 Package: [100 Units] Discontinued: 2023-04-05 Not in Commercial Distribution |
| GS1 | 10020221117308 [Package] Contains: 00020221117301 Package: CASE [100 Units] In Commercial Distribution |
| FPA | Set, Administration, Intravascular |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2023-04-06 |
| Device Publish Date | 2016-09-26 |
| 01002022117307 | IV Administration Set, Luer Slip, 1 injection site, 30" tubing |
| 10020221117209 | IV Administration Set, Luer Slip, 1 injection site, 20" tubing |
| 10020221017721 | IV Administration Set, 72" tubing |
| 10020221017301 | IV Administration Set, Luer Lock/Slip, 30" tubing |
| 00020221017205 | IV Administration Set, Luer Lock/Slip, 20" tubing |
| 10020221017127 | IV Administration Set, Luer Lock/Slip, 12" tubing |