| Primary Device ID | 60888937013483 |
| NIH Device Record Key | 6bed66d3-f4a9-4d23-88a9-1028948eb6fb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sales Demo Software |
| Version Model Number | 23485-SRD |
| Company DUNS | 801895244 |
| Company Name | Coopersurgical, 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 | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 60888937013483 [Primary] |
| FEM | Accessories, Photographic, For Endoscope (Exclude Light Sources) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-23 |
| 60888937029798 - ORIGIO Gradient 90 w/o Gentamicin | 2026-03-20 ORIGIO Gradient 90 w/o Gentamicin 5x60 ml |
| 00888937028331 - ORIGIO Sequential Blast | 2026-02-13 ORIGIO Sequential Blast. 10 ml |
| 00888937028348 - ORIGIO Sequential Blast | 2026-02-13 ORIGIO Sequential Blast 60 ml |
| 00888937028355 - ORIGIO Sequential Blast | 2026-02-13 ORIGIO Sequential Blast with phenol red. 10 ml |
| 00888937028386 - ORIGIO Sequential Cleav | 2026-02-13 ORIGIO Sequential Cleav. 10 ml |
| 00888937028393 - ORIGIO Sequential Cleav | 2026-02-13 ORIGIO Sequential Cleav. 60 ml |
| 00888937028409 - ORIGIO Sequential Cleav | 2026-02-13 ORIGIO Sequential Cleav with phenol red. 10 ml |
| 00888937028416 - ORIGIO Sequential Cleav | 2026-02-13 ORIGIO Sequential Cleav with phenol red. 60 ml |