| Primary Device ID | 10607915145351 |
| NIH Device Record Key | dd906f3e-83c0-40b0-b4e2-cfb7ba72e927 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GelPOINT V-Path |
| Version Model Number | C2C12 |
| Company DUNS | 187129135 |
| Company Name | APPLIED MEDICAL RESOURCES CORPORATION |
| 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 | false |
| 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 |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com | |
| Phone | 1-949-713-8300 |
| contact@appliedmedical.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10607915145351 [Primary] |
| MOK | Vaginoscope And Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-03-27 |
| Device Publish Date | 2023-03-17 |
| 10607915138667 | Transvaginal Access Platform |
| 10607915138490 | Transvaginal Access Platform |
| 10607915138483 | Transvaginal Access Platform |
| 00607915145613 | Transvaginal Access Platform |
| 10607915146693 | Transvaginal Access Platform with Insufflation Stabilization System |
| 10607915145368 | Transvaginal Access Platform with Total vNOTES Access System |
| 10607915145351 | Transvaginal Access Platform with Total vNOTES Access System |
| 10607915145344 | Transvaginal Access Platform with Total vNOTES Access System |
| 10607915145337 | Transvaginal Access Platform with Insufflation Stabilization System |
| 10607915145320 | Transvaginal Access Platform with Insufflation Stabilization System |
| 10607915145313 | Transvaginal Access Platform with Insufflation Stabilization System |