| Primary Device ID | 10840619033559 |
| NIH Device Record Key | a7c330c8-aa23-4993-af49-5d18d156fb27 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Transpac |
| Version Model Number | 42587-05 |
| Company DUNS | 118380146 |
| Company Name | ICU MEDICAL, INC. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840619033552 [Primary] |
| GS1 | 10840619033559 [Package] Contains: 00840619033552 Package: [20 Units] In Commercial Distribution |
| KRA | Catheter, continuous flush |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2019-12-11 |
| Device Publish Date | 2017-12-18 |
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