| Primary Device ID | 00817688020295 |
| NIH Device Record Key | 435236b1-52b6-4e6d-be5b-76b9d0248cff |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ultra Vac |
| Version Model Number | 2110-10 |
| Catalog Number | ICM-000-0480 |
| Company DUNS | 616182895 |
| Company Name | I.C. MEDICAL, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817688020288 [Primary] |
| GS1 | 00817688020295 [Package] Contains: 00817688020288 Package: [20 Units] In Commercial Distribution |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2019-04-08 |
| Device Publish Date | 2016-09-24 |
| 00817688020356 | 3110-10EC |
| 00817688020332 | 3110-10 |
| 00817688020318 | 2110-10EC |
| 00817688020295 | 2110-10 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ULTRA VAC 87124759 5325102 Live/Registered |
GHAZARIAN WELDING INC. 2016-08-02 |