| Primary Device ID | 50085412025365 |
| NIH Device Record Key | 69540e44-a99f-4488-9a49-15f26a1f0f57 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 5C4527 |
| Catalog Number | 5C4527 |
| Company DUNS | 005083209 |
| Company Name | BAXTER HEALTHCARE CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| 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 | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| 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 | |
| Phone | +1(800)933-0303 |
| MEDINFO_MEDPRODUCTS@BAXTER.COM |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00085412025360 [Primary] |
| GS1 | 50085412025365 [Package] Contains: 00085412025360 Package: CASE [12 Units] In Commercial Distribution |
| FKK | CLAMP, LINE |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-03-25 |
| Device Publish Date | 2019-03-15 |
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