| Primary Device ID | 20681490032173 |
| NIH Device Record Key | 1a01873a-80fc-4ede-9582-fa1b4e856a98 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hubbard |
| Version Model Number | 1056170 |
| Company DUNS | 835465063 |
| Company Name | MEDTRONIC XOMED, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 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 | 00681490032179 [Primary] |
| GS1 | 20681490032173 [Package] Contains: 00681490032179 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 | 2015-07-17 |
| 20681490032173 | VENT TUBE 1056170 5PK HUBBARD AIRPLANE |
| 20763000039565 | VENT TUBE 1056170 5PK HUBBARD AIRPLANE |
| 20763000282688 | VENT TUBE 1056170 5PK HUBBARD AIRPLANE |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HUBBARD 88778086 not registered Live/Pending |
Marcus Hubbard 2020-01-29 |
![]() HUBBARD 87727902 not registered Live/Pending |
Samuel Hubbard Shoe Company LLC 2017-12-20 |
![]() HUBBARD 86019224 not registered Dead/Abandoned |
Hubbard Shoe Company LLC 2013-07-24 |
![]() HUBBARD 86019220 not registered Dead/Abandoned |
Hubbard Shoe Company LLC 2013-07-24 |
![]() HUBBARD 86019217 not registered Dead/Abandoned |
Hubbard Shoe Company LLC 2013-07-24 |
![]() HUBBARD 77247046 3452570 Live/Registered |
RIDLEY USA INC. 2007-08-03 |
![]() HUBBARD 76579226 not registered Dead/Abandoned |
Hubbard, Kathleen M. 2004-02-27 |
![]() HUBBARD 76526019 2912218 Live/Registered |
HUBBARD 2003-06-17 |
![]() HUBBARD 74363563 1799089 Live/Registered |
Hubbard Jointers, Inc. 1993-02-25 |
![]() HUBBARD 74140345 1734728 Live/Registered |
Religious Technology Center 1991-02-19 |
![]() HUBBARD 73739943 1546167 Live/Registered |
RELIGIOUS TECHNOLOGY CENTER 1988-07-15 |
![]() HUBBARD 73702801 1505349 Live/Registered |
RELIGIOUS TECHNOLOGY CENTER 1987-12-28 |