| Primary Device ID | 24086000101268 |
| NIH Device Record Key | 4d533052-2935-497d-864e-32b9acb29f90 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Multi-Sampling Connector |
| Version Model Number | 4R5129 |
| Catalog Number | 4R5129 |
| Company DUNS | 315654579 |
| Company Name | Fresenius Kabi AG |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
| Special Storage Condition, Specify | Between 0 and 0 *Use once and destroy. Store at Room Temperature. Protect from freezing. Avoid excessive heat. |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04086000101240 [Primary] |
| GS1 | 14086000101254 [Package] Contains: 04086000101240 Package: Inner Pack [100 Units] In Commercial Distribution |
| GS1 | 24086000101268 [Package] Contains: 14086000101254 Package: Carton [20 Units] In Commercial Distribution |
| KST | System, Blood Collection, Vacuum-Assisted, Manual |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-10-23 |
| Device Publish Date | 2016-09-24 |
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