| Primary Device ID | 07290006558107 |
| NIH Device Record Key | 2616a3cd-54b6-4d2b-8f40-33e09f29ad64 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vagi-Screen Vaginal Health Test |
| Version Model Number | F-1-VO-VASC-02 |
| Company DUNS | 600850111 |
| Company Name | PEPTONIC MEDICAL ISRAEL LTD |
| Device Count | 2 |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290006558107 [Unit of Use] |
| GS1 | 17290006558104 [Primary] |
| CEN | Dye-Indicator, Ph (Urinary, Non-Quantitative) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-07-06 |
| Device Publish Date | 2023-06-28 |
| 07290006558091 - VagiVital VS | 2023-07-06 |
| 07290006558107 - Vagi-Screen Vaginal Health Test | 2023-07-06 |
| 07290006558107 - Vagi-Screen Vaginal Health Test | 2023-07-06 |
| 07290006558114 - Florisense Vaginal Health Test | 2023-07-06 |
| 07290006558121 - Florisense Preconception Vaginal Health Test | 2023-07-06 |
| 07290006558138 - Feminine Screening Kit | 2023-07-06 |
| 07290006558145 - Equate | 2023-07-06 |
| 07290006558152 - Clinistix Vaginal Health Test | 2023-07-06 |
| 07290006558169 - VS-SENSE | 2023-07-06 |