| Primary Device ID | 00840075404231 |
| NIH Device Record Key | 38883d91-58c7-4b7a-97dd-a7e85482d3b8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UltraCulture |
| Version Model Number | WVSP1104P200 |
| Catalog Number | WVSP1104P200 |
| Company DUNS | 609095955 |
| Company Name | Lonza Walkersville, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| 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 | 00840075404231 [Primary] |
| KIT | Media And Components, Synthetic Cell And Tissue Culture |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-03-20 |
| Device Publish Date | 2024-03-12 |
| 00840075404231 | WVSP1104P200 |
| 00840075404224 | WVSP1104P20 |
| 00840075404217 | WVSP1104P0.5 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ULTRACULTURE 97269738 not registered Live/Pending |
Ultraculture Incorporated 2022-02-16 |
![]() ULTRACULTURE 86365804 4780518 Live/Registered |
Ultraculture Incorporated 2014-08-13 |