| Primary Device ID | 04054839155017 |
| NIH Device Record Key | ed9528b3-3c4b-4504-a1fe-4ffd0f20f6dc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Minicon CS15 |
| Version Model Number | 9051 |
| Company DUNS | 896873994 |
| Company Name | MERCK MILLIPORE LIMITED |
| Device Count | 50 |
| 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 | true |
| 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 | 04054839155017 [Primary] |
| GS1 | 04054839155024 [Unit of Use] |
| JJH | Clinical Sample Concentrator |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-23 |
| 04053252359194 - Multiscreen-HTS HV | 2023-10-23 |
| 04053252466274 - Multiscreen-HTS HV | 2023-10-23 |
| 04053252504501 - Multiscreen-HV | 2023-10-23 |
| 04053252505928 - Multiscreen-HV | 2023-10-23 |
| 04061839736382 - Amicon Ultra – 15 | 2022-05-11 |
| 04061839736399 - Amicon Ultra – 4 | 2022-05-11 |
| 04061839736405 - Amicon Ultra – 15 | 2022-05-11 |
| 04061839736412 - Amicon Ultra – 4 | 2022-05-11 |