Primary Device ID | 08132500133826 |
NIH Device Record Key | 831ad987-3cc1-4b7c-9d29-e8620b3b531c |
Commercial Distribution Discontinuation | 2020-08-17 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Flextrode |
Version Model Number | FLEX-K151320-5P |
Company DUNS | 184200736 |
Company Name | COSMAN MEDICAL, LLC |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08132500133826 [Primary] |
GXI | Probe, Radiofrequency Lesion |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-08-18 |
Device Publish Date | 2016-10-07 |
08132500133826 - Flextrode | 2020-08-18Electrode 15cm, 13mm Tip, 20G |
08132500133826 - Flextrode | 2020-08-18 Electrode 15cm, 13mm Tip, 20G |
08132500158676 - tubingCTC | 2020-08-14 Tubing Set |
08132500159116 - tubingCTC | 2020-08-14 Ruler |
08132500159284 - electrodeCTC | 2020-08-14 Electrode 75mm |
08132500159352 - electrodeCTC | 2020-08-14 Electrode 150mm |
08132500159598 - cannulaCTC | 2020-08-14 Cannula 75mm, 4mm Tip, 17G |
08132500159734 - cannulaCTC | 2020-08-14 Cannula 150mm, 4mm Tip, 17G |
08132500160174 - cannulaEchoVU | 2020-08-14 Cannula 5cm, 5mm Tip, 21G |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() FLEXTRODE 77877857 4187161 Live/Registered |
Cosman, Eric Richard 2009-11-20 |
![]() FLEXTRODE 74360607 1797701 Dead/Cancelled |
AMREX-ZETRON, INC. 1993-02-22 |
![]() FLEXTRODE 73606651 1424722 Dead/Cancelled |
AMREX-ZETRON, INC. 1986-06-27 |