| Primary Device ID | 10816765014919 |
| NIH Device Record Key | e537e208-62d1-43ce-9326-f04e08349ab1 |
| Commercial Distribution Discontinuation | 2020-02-03 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | VIA |
| Version Model Number | 00717110 |
| Catalog Number | 00717110 |
| Company DUNS | 627879687 |
| Company Name | US Endoscopy |
| 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 | true |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816765014912 [Primary] |
| GS1 | 10816765014919 [Package] Contains: 00816765014912 Package: Box [20 Units] Discontinued: 2020-02-03 Not in Commercial Distribution |
| GS1 | 20816765014916 [Package] Contains: 00816765014912 Package: Case [18 Units] Discontinued: 2019-04-17 Not in Commercial Distribution |
| NWU | Endoscope introducer kit |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2020-02-03 |
| Device Publish Date | 2018-08-20 |
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