Primary Device ID | 00885556741962 |
NIH Device Record Key | 6da0814c-e096-47ce-bbb3-e1df055afc8f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Endo |
Version Model Number | E0016404-1 |
Catalog Number | E0016404-1 |
Company DUNS | 109903521 |
Company Name | Smith & Nephew, Inc. |
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 | 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 |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00885556741962 [Primary] |
FZX | Guide, surgical, instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00885556741962]
Moist Heat or Steam Sterilization
[00885556741962]
Moist Heat or Steam Sterilization
[00885556741962]
Moist Heat or Steam Sterilization
[00885556741962]
Moist Heat or Steam Sterilization
[00885556741962]
Moist Heat or Steam Sterilization
[00885556741962]
Moist Heat or Steam Sterilization
[00885556741962]
Moist Heat or Steam Sterilization
[00885556741962]
Moist Heat or Steam Sterilization
[00885556741962]
Moist Heat or Steam Sterilization
[00885556741962]
Moist Heat or Steam Sterilization
[00885556741962]
Moist Heat or Steam Sterilization
[00885556741962]
Moist Heat or Steam Sterilization
[00885556741962]
Moist Heat or Steam Sterilization
[00885556741962]
Moist Heat or Steam Sterilization
[00885556741962]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-04-10 |
Device Publish Date | 2019-04-02 |
00885556741092 | CURVED ARTHROPIERCE |
00885556741962 | DISTAL BICEP TENDON DRILL GUIDE |
00885556748510 | CURVED ARTHROPIERCE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ENDO 97188611 not registered Live/Pending |
Anderson Bell 2021-12-23 |
![]() ENDO 90855908 not registered Live/Pending |
Arnott T&P Holding, LLC 2021-07-29 |
![]() ENDO 90398429 not registered Live/Pending |
Agoric Systems Operating Company 2020-12-21 |
![]() ENDO 90118712 not registered Live/Pending |
Shade, Brendon 2020-08-17 |
![]() ENDO 90079225 not registered Live/Pending |
Endo Pharmaceuticals Inc. 2020-07-28 |
![]() ENDO 90055849 not registered Live/Pending |
Philip Bunting 2020-07-16 |
![]() ENDO 88346651 not registered Live/Pending |
Endo Pharmaceuticals Inc. 2019-03-19 |
![]() ENDO 87957172 not registered Dead/Abandoned |
DC Netcast Media Group 2018-06-11 |
![]() ENDO 87352763 5290576 Live/Registered |
Endo Tactical Inc. 2017-02-28 |
![]() ENDO 87352742 5290573 Live/Registered |
Endo Tactical Inc. 2017-02-28 |
![]() ENDO 86775932 5307112 Live/Registered |
Endo Pharmaceuticals Inc. 2015-10-02 |
![]() ENDO 86716698 not registered Dead/Abandoned |
Walter Contaldi 2015-08-06 |