| Primary Device ID | 50085412046360 |
| NIH Device Record Key | a6a1ed65-da85-40c5-a009-3605f4726caa |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CLEARLINK/DUO-VENT |
| Version Model Number | 2C8851 |
| Catalog Number | 2C8851 |
| Company DUNS | 005146311 |
| Company Name | BAXTER INTERNATIONAL INC. |
| 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 |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com | |
| Phone | +1(800)933-0303 |
| Medinfo_medproducts@baxter.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00085412046365 [Primary] |
| GS1 | 50085412046360 [Package] Contains: 00085412046365 Package: CASE [48 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 | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| 50085412565755 | Non-DEHP Solution Set with DUO-VENT Spike, 0.2 Micron Downstream Filter, Luer Activated Valve Ma |
| 50085412565632 | Solution Set with DUO-VENT Spike, Polyethylene Lined Tubing, Non-DEHP Pump Segment, Luer Activat |
| 50085412079757 | Solution Set with DUO-VENT Spike, Luer Activated Valve Male Luer Lock Adapter with Retractable C |
| 50085412049101 | Non-DEHP, Secondary Medication Set with DUO-VENT Spike, Hanger, Male Luer Lock Adapter |
| 50085412048951 | Solution Set with DUO-VENT Spike, Luer Activated Valve, Male Luer Lock Adapter with Retractable |
| 50085412048548 | Non-DEHP, Secondary Medication Set with DUO-VENT Spike, Hanger, Male Luer Lock Adapter |
| 50085412048494 | Non-DEHP Solution Set with DUO-VENT Spike, 0.2 Micron Downstream Filter, Luer Activated Valve, M |
| 50085412048470 | Secondary Medication Set with DUO-VENT Spike, Hanger, Male Luer Lock Adapter |
| 50085412046384 | Solution Set with DUO-VENT Spike, Polyethylene Lined Tubing, Non-DEHP Pump Segment, Luer Activat |
| 50085412046360 | Nitroglycerin Set with DUO-VENT Spike, PVC Tubing Segment, Luer Activated Valve, Male Luer Lock |