| Primary Device ID | 05407010125757 |
| NIH Device Record Key | ebd15907-813f-4f1b-8f70-a142a20c3f76 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ProVero™-1 NAO Med for Vero cells 500ml |
| Version Model Number | BESP1764F |
| Catalog Number | BESP1764F |
| 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 | 05407010125757 [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 | 2025-02-03 |
| Device Publish Date | 2025-01-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PROVERO 98322007 not registered Live/Pending |
Costello Training LLC 2023-12-19 |
![]() PROVERO 78784998 not registered Dead/Abandoned |
BHA Group, Inc. 2006-01-04 |