| 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 |
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| 60888937027206 - ERPeak | 2024-04-18 IVD Sample kit |
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