Primary Device ID | 10884450025427 |
NIH Device Record Key | 89900482-5f3a-4f9d-9943-3dbc6eeacf8d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ProGuide™ |
Version Model Number | 00884450025420 |
Catalog Number | DC21453631/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 | 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 |
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Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884450025420 [Primary] |
GS1 | 10884450025427 [Package] Contains: 00884450025420 Package: [5 Units] In Commercial Distribution |
MSD | Catheter, hemodialysis, implanted |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-31 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PROGUIDE 86516024 4862246 Live/Registered |
Merit Medical Systems, Inc. 2015-01-27 |
![]() PROGUIDE 76620214 not registered Dead/Abandoned |
Datascope Trademark Corp. 2004-11-12 |
![]() PROGUIDE 76375494 2807842 Dead/Cancelled |
T J SMITH & NEPHEW LMITED 2002-02-26 |
![]() PROGUIDE 75484907 2382190 Live/Registered |
PHASES INTERNATIONAL, LTD. 1998-05-14 |
![]() PROGUIDE 74039270 1712612 Dead/Cancelled |
Computer Aided Service, Inc. 1990-03-15 |