| Primary Device ID | 00366975024855 |
| NIH Device Record Key | 2b77c3fe-7fe5-46a4-9b37-e7ef8f83edb6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VISION XR |
| Version Model Number | 4232-242 |
| Company DUNS | 015108087 |
| Company Name | BENCO DENTAL SUPPLY CO. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| 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 | false |
| Phone | 570-602-6924 |
| jsoroka@benco.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00366975024855 [Primary] |
| IWZ | Film, Radiographic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-12-24 |
| Device Publish Date | 2018-11-21 |
| 00366975024930 | Vision XR Duplicating Film 6"x12"Box of 100 |
| 00366975024923 | Vision XR Duplicating Film 5"x12" Box of 100 |
| 00366975024916 | Vision XR Panoramic Film 6"x12" Box of 100 |
| 00366975024909 | Vision XR Panoramic Film 5"x12" Box of 100 |
| 00366975024893 | Vision XR Cephalometric Film 8"x10" Box of 100 |
| 00366975024886 | Vision XR Panoramic Film 6"x12" Box of 100 |
| 00366975024879 | Vision XR Intraoral Film Single FB-58 F-Speed Box of 150 |
| 00366975024862 | Vision XR Double FB-57 F-Speed Box of 150 |
| 00366975024855 | Vision XR Intraoral Film Single FB-54 F-Speed Box of 150 |
| 00366975024848 | Vision XR DB-58 D-Speed, Single Intraoral Film |
| 00366975024831 | Vision XR DB-57 D-Speed Double Intraoral Film |
| 00366975024824 | Vision XR Duplicating Film |