| Primary Device ID | 08057509880024 |
| NIH Device Record Key | d91db36b-98b6-425a-9123-4a064100aeaa |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | CO7026 |
| Company DUNS | 338946150 |
| Company Name | INGE SPA |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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 | 08057509880024 [Primary] |
| HGD | Applicator, Vaginal |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-07-25 |
| Device Publish Date | 2022-07-17 |
| 08057509880031 - NA | 2022-08-25 Kit including 21 cannulas for administering semi-solid preparation into the vagina |
| 08057509880024 - NA | 2022-07-25Cannulas for administering semi-solid preparation into the vagina |
| 08057509880024 - NA | 2022-07-25 Cannulas for administering semi-solid preparation into the vagina |