Primary Device ID | 00813110027306 |
NIH Device Record Key | 7b7468e9-1f79-4d12-a829-92a502deaa51 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Scan Post |
Version Model Number | 260-100-610 |
Catalog Number | 260-100-610 |
Company DUNS | 945015758 |
Company Name | BICON, LLC |
Device Count | 2 |
DM Exempt | false |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813110027306 [Primary] |
GS1 | 10813110027303 [Unit of Use] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-03-25 |
Device Publish Date | 2016-05-06 |
00813110027320 | 3.0mm Scan Post (2) |
00813110027313 | 2.5mm Scan Post (2) |
00813110027306 | 2.0mm Scan Post (2) |
00813110029768 | 3.0mm Titanium Scan Post (2) |
00813110029751 | 2.5mm Titanium Scan Post (2) |
00813110029744 | 2.0mm Titanium Scan Post (2) |