| Primary Device ID | 20681490105686 |
| NIH Device Record Key | 0d03fb61-143a-4c7d-b6e7-c1e3d51aa375 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Merocel® ELVIS® |
| Version Model Number | 400751 |
| Company DUNS | 835465063 |
| Company Name | MEDTRONIC XOMED, 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 | 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00681490105682 [Primary] |
| GS1 | 20681490105686 [Package] Contains: 00681490105682 Package: PK [10 Units] In Commercial Distribution |
| OCT | Anti fog solution and accessories, endoscopy |
| 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 | 2016-08-27 |
| 20681490105686 | CLEANER 400751 ELVIS 10PK ANTI-FOG |
| 20681490105679 | SPONGE 400750 ELVIS 10PK ANTI-FOG |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MEROCEL 90729765 not registered Live/Pending |
Medtronic Xomed, Inc. 2021-05-24 |
![]() MEROCEL 74441859 not registered Dead/Abandoned |
MEROCEL CORPORATION 1993-09-30 |
![]() MEROCEL 74439989 1910734 Live/Registered |
Medtronic Xomed, Inc. 1993-09-24 |
![]() MEROCEL 74439805 not registered Dead/Abandoned |
MEROCEL CORPORATION 1993-09-24 |
![]() MEROCEL 73078186 1051189 Live/Registered |
AMERICAL CORPORATION 1976-02-23 |