Primary Device ID | 08435452017337 |
NIH Device Record Key | f2d912f8-7025-4560-a49b-2f98a06d60d3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AVINENT |
Version Model Number | 4808 |
Company DUNS | 477451012 |
Company Name | AVINENT IMPLANT SYSTEM SLU |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08435452017337 [Primary] |
NDP | Accessories, implant, dental, endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08435452017337]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-09-23 |
Device Publish Date | 2019-09-13 |
08435452018488 | Scan Analog Prima PlusTM Ø5,0 CORE3D |
08435452018471 | Scan Analog Prima PlusTM Ø4,1 CORE3D |
08435452018464 | Scan Analog Prima PlusTM Ø3,5 CORE3D |
08435452018457 | Scan Analog Genesis Ø3,5 CORE3D |
08435452018440 | Scan Analog Prima PlusTM Ø6,0 CORE3D |
08435452018358 | Scan Analog TILOBEMAXXTM Ø8,0 CORE3D |
08435452018341 | Scan Analog TILOBEMAXXTM Ø7,0 CORE3D |
08435452018334 | Scan Analog Genesis Ø6,5 CORE3D |
08435452018327 | Scan Analog Genesis Ø5,5 CORE3D |
08435452018310 | Scan Analog Genesis Ø4,5 CORE3D |
08435452018303 | Scan Analog Genesis Ø3,8 CORE3D |
08435452018297 | Scan Analog PrimaConnex® Ø5,0 CORE3D |
08435452018280 | Scan Analog PrimaConnex® Ø4,1 CORE3D |
08435452018273 | Scan Analog PrimaConnex® Ø3,5 CORE3D |
08435452017405 | Scan Abutment Prima PlusTM Ø6,0 CORE3D |
08435452017399 | Scan Abutment Prima PlusTM Ø5,0 CORE3D |
08435452017382 | Scan Abutment Prima PlusTM Ø4,1 CORE3D |
08435452017375 | Scan Abutment Prima PlusTM Ø3,5 CORE3D |
08435452017368 | Scan Abutment TILOBEMAXXTM Ø8,0 CORE3D |
08435452017351 | Scan Abutment TILOBEMAXXTM Ø7,0 CORE3D |
08435452017344 | Scan Abutment Genesis Ø6,5 CORE3D |
08435452017337 | Scan Abutment Genesis Ø5,5 CORE3D |
08435452017320 | Scan Abutment Genesis Ø4,5 CORE3D |
08435452017313 | Scan Abutment Genesis Ø3,8 CORE3D |
08435452017306 | Scan Abutment Genesis Ø3,5 CORE3D |
08435452017290 | Scan Abutment PrimaConnex® Ø5,0 CORE3D |
08435452017283 | Scan Abutment PrimaConnex® Ø4,1 CORE3D |
08435452017276 | Scan Abutment PrimaConnex® Ø3,5 CORE3D |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AVINENT 88424146 not registered Live/Pending |
Avinent Implant System, S.L. 2019-05-10 |
AVINENT 86246511 not registered Live/Pending |
Avinent Canada Ltd. 2014-04-08 |