Primary Device ID | 00884450506011 |
NIH Device Record Key | 42ffc8df-434c-4aec-aa59-8449cf0e9e41 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Input® SSV |
Version Model Number | 10884450506018 |
Catalog Number | 808100 |
Company DUNS | 184763290 |
Company Name | Merit Medical Systems, Inc. |
Device Count | 5 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
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 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 | 00884450506011 [Unit of Use] |
GS1 | 10884450506018 [Primary] |
DYB | INTRODUCER, CATHETER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-08-09 |
Device Publish Date | 2021-07-30 |
00884450506059 | 10884450506056 |
00884450506035 | 10884450506032 |
00884450506028 | 10884450506025 |
00884450506011 | 10884450506018 |
00884450506004 | 10884450506001 |
00884450505991 | 10884450505998 |
00884450505984 | 10884450505981 |
00884450505946 | 10884450505943 |
00884450506042 | 10884450506049 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
INPUT 97447940 not registered Live/Pending |
El-Ghawaby, Mohab 2022-06-08 |
INPUT 88524916 not registered Live/Pending |
BDG Media, Inc. 2019-07-19 |
INPUT 87978649 5603411 Live/Registered |
Input Tech, Inc. 2017-02-24 |
INPUT 87349048 not registered Live/Pending |
Input Tech, Inc. 2017-02-24 |
INPUT 87017908 not registered Dead/Abandoned |
Peter Cunningham 2016-04-28 |
INPUT 86217526 4617376 Live/Registered |
THE FONT BUREAU INC. 2014-03-11 |
INPUT 79289760 not registered Live/Pending |
SEI-HEI MOON, S.L. 2020-06-19 |
INPUT 78203132 2788957 Dead/Cancelled |
INPUT, INC. 2003-01-14 |
INPUT 77770848 3990598 Dead/Cancelled |
Krueger International, Inc. 2009-06-30 |
INPUT 76714207 4479134 Live/Registered |
TIMES FIBER COMMUNICATIONS, INC. 2013-05-23 |
INPUT 76188467 2946849 Live/Registered |
Gallup, Inc. 2001-01-02 |
INPUT 75605621 2468218 Dead/Cancelled |
Punch Products USA, Inc. 1998-12-14 |