Primary Device ID | 04560218661579 |
NIH Device Record Key | 2d211e67-792e-48ef-8c24-a6ec2ab3cfdf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DENTECH |
Version Model Number | 01023020 |
Company DUNS | 700723000 |
Company Name | DENTECH CORPORATION |
Device Count | 1 |
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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04560218661579 [Primary] |
EIE | Dam, Rubber |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-29 |
Device Publish Date | 2020-07-21 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() DENTECH 97623306 not registered Live/Pending |
Forsyth Dental Infirmary For Children 2022-10-07 |
![]() DENTECH 79183905 not registered Dead/Abandoned |
DENTECH CORPORATION 2015-11-09 |
![]() DENTECH 75156931 not registered Dead/Abandoned |
Focused Energy International, Inc. 1996-08-28 |
![]() DENTECH 74035454 1810628 Live/Registered |
DENTECH PRODUCTS LTD. 1990-02-27 |