| Primary Device ID | 00846338001124 |
| NIH Device Record Key | eeb16d3d-2338-4471-a28b-f66647326e7b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FlexTrode® Malleable Electrode |
| Version Model Number | FT-W/S |
| Company DUNS | 019872358 |
| Company Name | ELLIQUENCE, 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00846338001124 [Primary] |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2016-09-22 |
| 00846338001124 | FT-W/S |
| 00846338001117 | FT-S/S |
| 00846338001094 | FT-N/S |
| 00846338001087 | FT-L7/S |
| 00846338001070 | FT-L5/S |
| 00846338001063 | FT-L3/S |
| 00846338001056 | FT-D/S |
| 00846338001049 | FT-B3/S |
| 00846338001032 | FT-B2/S |
| 00846338001025 | FT-B1/S |
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 |