Primary Device ID | M20655760 |
NIH Device Record Key | b372c2cf-5a19-4806-a96e-bfdb87e4374b |
Commercial Distribution Discontinuation | 2018-11-17 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | GuideLiner® XL catheter |
Version Model Number | 5576 |
Company DUNS | 008999906 |
Company Name | Vascular Solutions, 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 | true |
OTC Over-The-Counter | false |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Catheter Gauge | 6 French |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M20655760 [Primary] |
DQY | Catheter, Percutaneous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 7 |
Public Version Date | 2019-11-11 |
Device Publish Date | 2016-09-05 |
M20677101 - Vascular Solutions Custom Access Kit | 2023-06-09 |
M20677141 - Vascular Solutions Custom Access Kit | 2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following |
M20677181 - Vascular Solutions Custom Access Kit | 2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following |
M20677191 - Vascular Solutions Custom Access Kit | 2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following |
M20677201 - Vascular Solutions Custom Access Kit | 2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following |
M20677211 - Vascular Solutions Custom Access Kit | 2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following |
M20677221 - Vascular Solutions Custom Access Kit | 2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following |
M20677231 - Vascular Solutions Custom Access Kit | 2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GUIDELINER 78602801 not registered Dead/Abandoned |
Vascular Solutions, Inc. 2005-04-06 |
GUIDELINER 78449779 not registered Dead/Abandoned |
Johnson & Johnson 2004-07-13 |
GUIDELINER 77706364 3797195 Live/Registered |
TELEFLEX INNOVATIONS S.Ã R.L. 2009-04-03 |
GUIDELINER 74022839 1621008 Dead/Cancelled |
Andrew Corporation 1990-01-26 |