Primary Device ID | 40841156109111 |
NIH Device Record Key | da49d42d-55b2-462c-8635-bc7590147ae7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GUIDELINER |
Version Model Number | IPN929286 |
Catalog Number | 5570 |
Company DUNS | 002348191 |
Company Name | TELEFLEX INCORPORATED |
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 | true |
OTC Over-The-Counter | false |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Catheter Gauge | 5.5 French |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10841156109110 [Previous] |
GS1 | 30841156109114 [Primary] |
GS1 | 40841156109111 [Package] Contains: 30841156109114 Package: Box [1 Units] In Commercial Distribution |
DQY | Catheter, percutaneous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-24 |
Device Publish Date | 2024-04-16 |
30841156100647 | GuideLiner V3 8F |
30841156100623 | GuideLiner V3 7F |
30841156100609 | GuideLiner V3 6F |
30841156100586 | GuideLiner V3 5.5F |
30841156100579 | GuideLiner V3 5F |
20841156106567 | GuideLiner V3 6F |
20841156109117 | GuideLiner V3 5.5F |
20841156109124 | GuideLiner V3.5 6F |
20841156108950 | GuideLiner Coast,3.5,5.5F |
20841156108943 | GuideLiner Coast,3.5,8F |
20841156108936 | GuideLiner Coast,3.5,7F |
20841156108929 | GuideLiner Coast,3.5,6F |
20841156109148 | GuideLiner 8F |
20841156109131 | GuideLiner 7F |
20841156109100 | GuideLiner 5F |
40841156109111 | GuideLiner V3 5.5F |
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 |