Primary Device ID | D76845000K0 |
NIH Device Record Key | 69095e23-834b-44e5-bc0c-a88df791c275 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Prima |
Version Model Number | 45000K |
Catalog Number | 45000K |
Company DUNS | 787471015 |
Company Name | KEYSTONE DENTAL, INC. |
Device Count | 1 |
DM Exempt | true |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com | |
Phone | +1(866)902-9272 |
info@keystonedental.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D76845000K0 [Primary] |
NHA | ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2021-03-31 |
Device Publish Date | 2016-02-04 |