Primary Device ID | 00817688020967 |
NIH Device Record Key | b38744f9-24f0-4f79-a747-404ed75114ae |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Electrode |
Version Model Number | ICM-000-0249 |
Company DUNS | 616182895 |
Company Name | I.C. MEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817688020950 [Primary] |
GS1 | 00817688020967 [Package] Contains: 00817688020950 Package: [5 Units] In Commercial Distribution |
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 | 6 |
Public Version Date | 2019-04-08 |
Device Publish Date | 2016-09-24 |
00817688021049 | ICM-000-0334 |
00817688021025 | ICM-000-0332 |
00817688021001 | ICM-000-0330 |
00817688020981 | ICM-000-0251 |
00817688020967 | ICM-000-0249 |
00817688020943 | ICM-000-0245 |
00817688020929 | ICM-000-0242 |
00817688020905 | ICM-000-0215 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ELECTRODE 87012659 not registered Live/Pending |
Wal-Mart Stores, Inc 2016-04-25 |
ELECTRODE 87012643 not registered Live/Pending |
Wal-Mart Stores, Inc 2016-04-25 |
ELECTRODE 85132625 not registered Dead/Abandoned |
Ball, Michael 2010-09-17 |