| Primary Device ID | 50085412676635 |
| NIH Device Record Key | 63c6e48d-2286-430c-bdb0-a7751110dbe9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DUO - DUO-VENT |
| Version Model Number | 2R8404 |
| Catalog Number | 2R8404 |
| 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 |
| 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 |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Total Volume | 5.9 Milliliter |
| Length | 1.1 Meter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00085412676630 [Primary] |
| GS1 | 50085412676635 [Package] Contains: 00085412676630 Package: CA [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 | 2023-07-19 |
| Device Publish Date | 2023-07-11 |
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