| Primary Device ID | 50197886004361 |
| NIH Device Record Key | defab711-2e27-4d79-ba27-f493c76b012a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CLEARLINK/CONTINU-FLO |
| Version Model Number | ALT2402 |
| Catalog Number | ALT2402 |
| Company DUNS | 005083209 |
| Company Name | BAXTER HEALTHCARE CORPORATION |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com | |
| Phone | +1(800)933-0303 |
| US-MEDINFO_MEDPRODUCTS@baxter.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00197886004366 [Primary] |
| GS1 | 50197886004361 [Package] Contains: 00197886004366 Package: Case [48 Units] In Commercial Distribution |
| FPA | Set, administration, intravascular |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-06-10 |
| Device Publish Date | 2024-05-31 |
| 51978860004367 | QuickStay Set, 24 Hour Max Use, For Gravity Use Only, Clearlink System, Non-DEHP Continu-Flo Sol |
| 51978860004350 | QuickStay Set, 24 Hour Max Use, For Gravity Use Only, Clearlink System, Non-DEHP Continu-Flo Sol |
| 50197886004361 | QuickStay Set, 24 Hour Max Use, For Gravity Use Only, Clearlink System, Non-DEHP Continu-Flo Sol |
| 50197886004354 | QuickStay Set, 24 Hour Max Use, For Gravity Use Only, Clearlink System, Non-DEHP Continu-Flo Sol |