Primary Device ID | 00852550007233 |
NIH Device Record Key | 8442a3ff-a747-45a5-bcdd-25d0d75c4a67 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 16 MM ULTRA TOOTH IMPLANT |
Version Model Number | 3916UT |
Company DUNS | 017725036 |
Company Name | Bio-Dent, 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 | false |
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 |
Height | 16 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852550007233 [Primary] |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-12-22 |
00852550007165 - 8mm ULTRA TOOTH SOLID WIDE IMPLANT | 2018-07-06 |
00852550007172 - 10 MM ULTRA TOOTH SOLID WIDE IMPLANT | 2018-07-06 |
00852550007189 - 13 MM ULTRA TOOTH SOLID WIDE IMPLANT | 2018-07-06 |
00852550007196 - 16 MM ULTRA TOOTH SOLID WIDE IMPLANT | 2018-07-06 |
00852550007202 - 8 MM ULTRA TOOTH IMPLANT | 2018-07-06 |
00852550007219 - 10 MM ULTRA TOOTH IMPLANT | 2018-07-06 |
00852550007226 - 13 MM ULTRA TOOTH IMPLANT | 2018-07-06 |
00852550007233 - 16 MM ULTRA TOOTH IMPLANT | 2018-07-06 |
00852550007233 - 16 MM ULTRA TOOTH IMPLANT | 2018-07-06 |