| Primary Device ID | 50085412676642 |
| NIH Device Record Key | a57d4d58-b687-428c-90ca-26837ed56bb1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CLEARLINK/CONTINU-FLO/DUO-VENT |
| Version Model Number | 2R8538 |
| Catalog Number | 2R8538 |
| 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 |
| Length | 119 Inch |
| Total Volume | 13 Milliliter |
| Length | 119 Inch |
| Total Volume | 13 Milliliter |
| Length | 119 Inch |
| Total Volume | 13 Milliliter |
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| Total Volume | 13 Milliliter |
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| Total Volume | 13 Milliliter |
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| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00085412676647 [Primary] |
| GS1 | 50085412676642 [Package] Contains: 00085412676647 Package: CASE [48 Units] Discontinued: 2040-12-31 In Commercial Distribution |
| FPA | Set, Administration, Intravascular |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-03-29 |
| Device Publish Date | 2021-03-19 |
| 50085412676642 | CLEARLINK System Solution Set with DUO-VENT Spike |
| 50085412729263 | Non-DEHP CONTINU-FLO Solution Set with DUO-VENT Spike, 2 Luer Activated Valves, Male Luer Lock A |
| 50085412729188 | Non-DEHP CONTINU-FLO Solution Set with DUO-VENT Spike, 3 Luer Activated Valves, Male Luer Lock A |