Primary Device ID | 00366975024893 |
NIH Device Record Key | e3e29cde-73cb-43e5-a5fa-924272a04ce1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VISION XR |
Version Model Number | 4232-288 |
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 | 00366975024893 [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 | 2018-12-31 |
Device Publish Date | 2018-11-28 |
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 |