Primary Device ID | 10884450297879 |
NIH Device Record Key | 7a658711-04ca-424d-8aa2-4304c899fd9b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | True Form™ |
Version Model Number | 00884450297872 |
Catalog Number | TF14165S/A |
Company DUNS | 184763290 |
Company Name | Merit Medical Systems, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | 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 |
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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 | 00884450297872 [Primary] |
GS1 | 10884450297879 [Package] Contains: 00884450297872 Package: [5 Units] In Commercial Distribution |
DQX | Wire, guide, catheter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-03-22 |
Device Publish Date | 2017-10-16 |
10884450297893 | 00884450297896 |
10884450297886 | 00884450297889 |
10884450297879 | 00884450297872 |
10884450297862 | 00884450297865 |
10884450297848 | 00884450297841 |
10884450329761 | 00884450329764 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() TRUE FORM 98700618 not registered Live/Pending |
Vision LLC 2024-08-15 |
![]() TRUE FORM 90236621 not registered Live/Pending |
Express Recycling & Collections Inc 2020-10-05 |
![]() TRUE FORM 87420855 5499097 Live/Registered |
Merit Medical Systems, Inc. 2017-04-21 |
![]() TRUE FORM 85533441 4332727 Dead/Cancelled |
TRUE FORM, LLC 2012-02-03 |
![]() TRUE FORM 79234913 not registered Dead/Abandoned |
LARY S.a.r.l. 2018-05-18 |
![]() TRUE FORM 78018556 not registered Dead/Abandoned |
Ball Screws & Actuators Co., Inc. 2000-07-27 |
![]() TRUE FORM 73804175 1577556 Dead/Cancelled |
ADOBE SYSTEMS INCORPORATED 1989-06-01 |
![]() TRUE FORM 71188871 0186657 Dead/Cancelled |
True Form Corset Co. 1923-11-24 |