| Primary Device ID | 00681490034678 |
| NIH Device Record Key | f5d7db14-71d9-4b7d-996f-5fb508c8dc67 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Lippy |
| Version Model Number | 1133295 |
| 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 |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| 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 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 5.5 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00681490034678 [Primary] |
| ETA | REPLACEMENT, OSSICULAR PROSTHESIS, TOTAL |
| 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 | 2015-06-23 |
| 00681490669771 | PROSTHESIS 1133265 LIPPY CUP PSTN .6X5.5 |
| 00681490034685 | PROSTHESIS 1133300 LIPPY CUP PSTN .4X6.0 |
| 00681490034678 | PROSTHESIS 1133295 LIPPY CUP PSTN .4X5.5 |
| 00681490034661 | PROSTHESIS 1133290 LIPPY CUP PSTN .4X5.0 |
| 00681490034654 | PROSTHESIS 1133285 LIPPY CUP PSTN .4X4.5 |
| 00681490034647 | PROSTHESIS 1133280 LIPPY CUP PSTN .4X4.0 |
| 00681490034630 | PROSTHESIS 1133270 LIPPY CUP PSTN .6X6.0 |
| 00681490034623 | PROSTHESIS 1133260 LIPPY CUP PSTN .6X5.0 |
| 00681490034616 | PROSTHESIS 1133255 LIPPY CUP PSTN .6X4.5 |
| 00681490034609 | PROSTHESIS 1133250 LIPPY CUP PSTN .6X4.0 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LIPPY 90326128 not registered Live/Pending |
Amron, David 2020-11-18 |
![]() LIPPY 88618356 not registered Live/Pending |
LIPPY LLC 2019-09-16 |
![]() LIPPY 78305207 not registered Dead/Abandoned |
998232 Alberta Ltd. 2003-09-25 |
![]() LIPPY 78305203 not registered Dead/Abandoned |
998232 Alberta Ltd. 2003-09-25 |
![]() LIPPY 77710238 not registered Dead/Abandoned |
Robert P. Nickell 2009-04-09 |
![]() LIPPY 73477465 1323316 Dead/Cancelled |
Pretty Industries, Inc. 1984-04-26 |