Primary Device ID | 10886333212191 |
NIH Device Record Key | eb918b6b-88ae-4200-b471-be262d7349dc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Guidewire |
Version Model Number | 395946 |
Catalog Number | 395946 |
Company DUNS | 140727624 |
Company Name | ARGON MEDICAL DEVICES, 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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00886333212194 [Primary] |
GS1 | 10886333212191 [Package] Contains: 00886333212194 Package: Box [10 Units] In Commercial Distribution |
GS1 | 20886333212198 [Package] Contains: 00886333212194 Package: Box [50 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 | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-20 |
10886333221179 | Guidewire 25/260/FC/PTFE/1.5J |
10886333221162 | Guidewire 25/150/FC/PTFE/DE-1.5J< |
10886333216328 | Guidewire 32/150/FC/PTFE/1.5J |
10886333216311 | Guidewire 35/150/FC/PTFE/1.5J |
10886333216304 | Guidewire 35/200/FC/PTFE/3J |
10886333216298 | Guidewire 32/125/FC/PTFE/3J |
10886333216281 | Guidewire 32/150/FC/PTFE/3J |
10886333216274 | Guidewire 25/150/FC/PTFE/3J |
10886333216267 | Guidewire 35/180/FC/PTFE/3J |
10886333216250 | Guidewire 35/260/FC/PTFE/ST |
10886333216243 | Guidewire 35/150/Movable Core/PTFE/3J/HD |
10886333216236 | Guidewire 38/150/FC/PTFE/3J |
10886333216229 | Guidewire 35/150/FC/PTFE/3J |
10886333216212 | Guidewire 35/150/FC/PTFE/ST |
10886333212290 | Guidewire 35/50/FC/PTFE/DE/3J&ST |
10886333212276 | Guidewire 35/150/FC/PTFE/3J/HD |
10886333212269 | Guidewire 30/150/FC/PTFE/3J |
10886333212252 | Guidewire 28/50/FC/DE/3J&ST |
10886333212245 | Guidewire 17/150/FC/Mullins |
10886333212238 | Guidewire 15/150/FC/Mullins |
10886333212221 | Guidewire 28/40/FC/ST |
10886333212214 | Guidewire 28/150/FC/PTFE/3J |
10886333212207 | Guidewire 21/100/FC/Mullins/2cm Soft Tip |
10886333212191 | Guidewire 21/65/FC/Mullins/2cm Soft Tip |
10886333212184 | Guidewire 18/100/FC/Mullins/2cm Soft Tip |
10886333212177 | Guidewire 18/65/FC/Mullins/2cm Soft Tip |
10886333212160 | Guidewire 38/150/FC/PTFE/BENTSON |
10886333212153 | Guidewire 32/150/FC/PTFE/BENTSON |
10886333212146 | Guidewire 35/150/FC/PTFE/BENTSON |
10886333212139 | Guidewire 38/80/FC/3J |
10886333212122 | Guidewire 35/150/FC/PTFE/DE/LT&1.5J |
10886333212115 | Guidewire 32/150/FC/PTFE/1.5J |
10886333212108 | Guidewire 35/65/FC/DE/3J&ST |
10886333212092 | Guidewire 28/150/FC/PTFE/ST |
10886333212085 | Guidewire 25/65/FC/ST |
10886333212078 | Guidewire 21/65/FC/PTFE/ST |
10886333212061 | Guidewire 18/65/FC/PTFE/ST |
10886333212054 | Guidewire 35/80/FC/DE/3J&ST |
10886333212047 | Guidewire 38/150/FC/PTFE/1.5J |
10886333212030 | Guidewire 38/50/FC/DE/3J&ST |
10886333212023 | Guidewire 38/70/FC/ST |
10886333212016 | Guidewire 38/260/FC/PTFE/3J |
10886333212009 | Guidewire 38/60/FC/3J |
10886333211996 | Guidewire 38/50/FC/3J |
10886333211989 | Guidewire 38/200/FC/PTFE/3J |
10886333211972 | Guidewire 35/70/FC/3J |
10886333211965 | Guidewire 35/260/FC/PTFE/3J |
10886333211958 | Guidewire 35/150/FC/PTFE/1.5J |
10886333211941 | Guidewire 35/150/FC/PTFE/7.5J |
10886333211934 | Guidewire 35/50/FC/ST |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GUIDEWIRE 87540652 5401314 Live/Registered |
Guidewire Software, Inc. 2017-07-24 |
GUIDEWIRE 78662211 3185991 Live/Registered |
Guidewire Software, Inc. 2005-06-30 |
GUIDEWIRE 77016329 3273576 Dead/Cancelled |
Yu, Steven S. 2006-10-07 |
GUIDEWIRE 76474094 not registered Dead/Abandoned |
GUIDEWIRE SYSTEMS, INC. 2002-12-12 |