| Primary Device ID | 05407010128642 |
| NIH Device Record Key | 752b71a2-7391-456e-88e1-1849751110f5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TSB 3%:10 L bag (empty bag capacity) |
| Version Model Number | BESP1795P10 |
| Catalog Number | BESP1795P10 |
| Company DUNS | 370158847 |
| Company Name | Lonza Verviers |
| 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 | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 | 05407010128642 [Primary] |
| JSD | Culture Media, Selective Broth |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-09-23 |
| Device Publish Date | 2025-09-15 |
| 05407010129656 - CD CHO Medium AGT-200Lbag filled to 100L | 2025-11-21 |
| 05407010129403 - KH-020 BF-6 1L Bag - Sample | 2025-11-19 |
| 05407010129410 - KH-020 BF-8 1L Sample Bag | 2025-11-19 |
| 05407010129427 - KH-020 BF-8 1000L Bag | 2025-11-19 |
| 05407010129434 - KH-020 BF-8 500L Bag | 2025-11-19 |
| 05407010129441 - KH-020 BF-9 1000L Bag | 2025-11-19 |
| 05407010129458 - KH-020 BF-9 1L Sample Bag | 2025-11-19 |
| 05407010129465 - KH-020 BF-9 500L Bag | 2025-11-19 |