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 |