| Primary Device ID | 20814247020615 |
| NIH Device Record Key | 6e0cf12e-6a26-4856-a285-aa184e9c762c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ClearView Total Uterine Manipulator |
| Version Model Number | UM950 |
| Company DUNS | 809524291 |
| Company Name | CLINICAL INNOVATIONS, LLC |
| 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 | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00814247020611 [Primary] |
| GS1 | 10814247020618 [Package] Contains: 00814247020611 Package: [5 Units] In Commercial Distribution |
| GS1 | 20814247020615 [Package] Contains: 10814247020618 Package: [4 Units] In Commercial Distribution |
| LKF | Cannula, Manipulator/Injector, Uterine |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-01 |
| 20814247020615 | ClearView Total Uterine Manipulator, 9cm tip |
| 00814247020499 | ClearView Total Uterine Manipulator, regular tip (7cm) |