Primary Device ID | D7701304933 |
NIH Device Record Key | aedc9461-4dc2-413a-8cf9-c008499a805a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KOHNO ONE IMPLANT ZIRTI |
Version Model Number | KS-ZT-500-100 |
Catalog Number | KS-ZT-500-100 |
Company DUNS | 433815198 |
Company Name | SWEDEN & MARTINA SPA |
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 | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 844.862.7846 |
info.us@sweden-martina.com | |
Phone | 844.862.7846 |
info.us@sweden-martina.com | |
Phone | 844.862.7846 |
info.us@sweden-martina.com | |
Phone | 844.862.7846 |
info.us@sweden-martina.com | |
Phone | 844.862.7846 |
info.us@sweden-martina.com | |
Phone | 844.862.7846 |
info.us@sweden-martina.com | |
Phone | 844.862.7846 |
info.us@sweden-martina.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D7701304933 [Primary] |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-07 |
Device Publish Date | 2022-06-29 |
D7701304953 | KOHNO ONE IMPLANT ZIRTI ZT D.5.00 H.13 MM |
D7701304943 | KOHNO ONE IMPLANT ZIRTI ZT D.5.00 H.11.5 MM |
D7701304933 | KOHNO ONE IMPLANT ZIRTI ZT D.5.00 H.10 MM |
D7701304923 | KOHNO ONE IMPLANT ZIRTI ZT D.4.25 H.18 MM |
D7701304913 | KOHNO ONE IMPLANT ZIRTI ZT D.4.25 H.15 MM |
D7701304903 | KOHNO ONE IMPLANT ZIRTI ZT D.4.25 H.13 MM |
D7701304893 | KOHNO ONE IMPLANT ZIRTI ZT D.4.25 H.11.5 MM |
D7701304883 | KOHNO ONE IMPLANT ZIRTI ZT D.4.25 H.10 MM |