| Primary Device ID | 20681490031947 |
| NIH Device Record Key | 8d8ba8f4-2334-49d8-a03c-19ebe8391336 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tytan® |
| Version Model Number | 1056102 |
| Company DUNS | 835465063 |
| Company Name | MEDTRONIC XOMED, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| 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 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 Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00681490031943 [Primary] |
| GS1 | 20681490031947 [Package] Contains: 00681490031943 Package: PK [5 Units] In Commercial Distribution |
| ETD | TUBE, TYMPANOSTOMY |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2015-07-13 |
| 20681490032548 | VENT TUBE 1066106 10PK SPOON BOB PR 1.27 |
| 20681490031992 | VENT TUBE 1056109 5PK SPOON BOBB TYTAN |
| 20681490031961 | VENT TUBE 1056106 5PK SPOON BOBB TYTAN |
| 20681490031947 | VENT TUBE 1056102 5PK TYTAN PED .76MM |
| 20681490031930 | VENT TUBE 1056101 5PK TYTAN PED .76MM |
| 20763000039428 | VENT TUBE 1056109 5PK SPOON BOBB TYTAN |
| 20763000039381 | VENT TUBE 1056102 5PK TYTAN PED .76MM |
| 20763000039374 | VENT TUBE 1056101 5PK TYTAN PED .76MM |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TYTAN 97614247 not registered Live/Pending |
Lone Star Merchandising Group Inc. 2022-09-30 |
![]() TYTAN 97173643 not registered Live/Pending |
NAI International Group, Inc. 2021-12-15 |
![]() TYTAN 88577921 not registered Live/Pending |
Lone Star Merchandising Group, Inc. 2019-08-14 |
![]() TYTAN 87509820 5542318 Live/Registered |
Meshram Pratik 2017-06-28 |
![]() TYTAN 79399872 not registered Live/Pending |
Ruroc IP Holdings Limited 2024-05-02 |
![]() TYTAN 78673845 3555293 Live/Registered |
BORICA CO., LTD 2005-07-19 |
![]() TYTAN 77277639 3519158 Live/Registered |
SELENA MARKETING INTERNATIONAL SP. Z O.O 2007-09-12 |
![]() TYTAN 76615028 not registered Dead/Abandoned |
Budge Industries LLC 2004-10-06 |
![]() TYTAN 76386416 not registered Dead/Abandoned |
Selena USA, Inc. 2002-03-25 |
![]() TYTAN 74626063 not registered Dead/Abandoned |
XOMED-TREACE, INC. 1995-01-26 |
![]() TYTAN 74626062 2796410 Live/Registered |
Medtronic Xomed, Inc. 1995-01-26 |
![]() TYTAN 73717435 not registered Dead/Abandoned |
LAMSON & SESSIONS CO., THE 1988-03-18 |