Primary Device ID | 00885556632710 |
NIH Device Record Key | d29570dd-e738-4859-9a24-4c652c0faf83 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WEREWOLF |
Version Model Number | 72290066 |
Catalog Number | 72290066 |
Company DUNS | 109903521 |
Company Name | Smith & Nephew, Inc. |
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 | 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 | |
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 | 00885556632710 [Primary] |
GEI | Electrosurgical, cutting & coagulation & accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2018-05-30 |
00885556632710 | WEREWOLF POWER CORD/MANUAL - CHINA |
00885556632628 | WEREWOLF POWER CORD/MANUAL - US ENGLISH |
00885556692516 | WEREWOLF MAIN SW UPGRADE V. 2.6-3.0 |
00885556739624 | WEREWOLF ENT |
00885556775592 | ENT RF20000 CONTROLLER REFURBISHED |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
WEREWOLF 98745937 not registered Live/Pending |
Tundra Labs LLC 2024-09-11 |
WEREWOLF 98423543 not registered Live/Pending |
Fecon, LLC 2024-02-27 |
WEREWOLF 98290834 not registered Live/Pending |
PSYMETIS, INC. 2023-11-29 |
WEREWOLF 88698485 not registered Live/Pending |
Werewolf Therapeutics, Inc. 2019-11-19 |
WEREWOLF 87295394 not registered Dead/Abandoned |
DMK Management, LLC 2017-01-10 |
WEREWOLF 87015233 5234972 Live/Registered |
KIND PET PRODUCTS (DALIAN) CO.,LTD 2016-04-26 |
WEREWOLF 86700913 5110685 Live/Registered |
Smith & Nephew, Inc. 2015-07-22 |
WEREWOLF 78589623 not registered Dead/Abandoned |
Clark, Ronald J. 2005-03-17 |
WEREWOLF 78586489 3102291 Live/Registered |
Tri Vin Imports, Inc. 2005-03-14 |
WEREWOLF 77420169 3515832 Dead/Cancelled |
Rubie's Costume Co., Inc. 2008-03-12 |
WEREWOLF 74692862 not registered Dead/Abandoned |
Aegis Entertainment, Inc. 1995-06-23 |
WEREWOLF 74479682 not registered Dead/Abandoned |
NOVALOGIC, INC. 1994-01-10 |