| Primary Device ID | 10886333216205 |
| NIH Device Record Key | f4187b43-0e55-4096-8154-64b257f23d5a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vessel Dilator |
| Version Model Number | A392306 |
| Catalog Number | A392306 |
| Company DUNS | 140727624 |
| Company Name | ARGON MEDICAL DEVICES, INC. |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| 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 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 Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00886333216208 [Primary] |
| GS1 | 10886333216205 [Package] Contains: 00886333216208 Package: Box [10 Units] In Commercial Distribution |
| DRE | Dilator, Vessel, For Percutaneous Catheterization |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-06-07 |
| Device Publish Date | 2016-09-20 |
| 10886333216205 | Vessel Dilator with Feathered Tip 7 French |
| 10886333210432 | Vessel Dilator 4 French |
| 10886333210425 | Vessel Dilator 5 French |
| 10886333210418 | Vessel Dilator 9 French |
| 10886333210401 | Vessel Dilator 8 French |
| 10886333210395 | Vessel Dilator 8 French |
| 10886333210388 | Vessel Dilator 7 French |
| 10886333210371 | Vessel Dilator 6 French |
| 10886333210364 | Vessel Dilator 6 French |
| 10886333210357 | Vessel Dilator 5 French |
| 10886333210340 | Vessel Dilator 5 French |
| 10886333210333 | Vessel Dilator 4 French |
| 10886333210326 | Vessel Dilator 4 French |
| 10886333210319 | Vessel Dilator 4 French |