Primary Device ID | 00811478011906 |
NIH Device Record Key | 78fc4609-7626-4f8b-9f6c-88a325d5b1d8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ELECTRO-GEL 128OZ |
Version Model Number | E11 |
Catalog Number | E11 |
Company DUNS | 186765806 |
Company Name | ELECTRO-CAP INTERNATIONAL 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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 | 18005272193 |
eci@electro-cap.com | |
Phone | 18005272193 |
eci@electro-cap.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00811478011906 [Primary] |
GYB | Media, Electroconductive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-10-22 |
Device Publish Date | 2016-09-23 |
00811478010213 - NEEDLE/SYRINGE KIT - LARGE | 2020-12-16 |
00811478011883 - ELECTRO-GEL 16oz | 2018-10-22 |
00811478011890 - ELECTRO-GEL 32oz | 2018-10-22 |
00811478011906 - ELECTRO-GEL 128OZ | 2018-10-22 |
00811478011906 - ELECTRO-GEL 128OZ | 2018-10-22 |
00811478011913 - ELECTRO-GEL 16OZ. BOXED | 2018-10-22 |
00811478011920 - ELECTRO-GEL 32 OZ. BOXED | 2018-10-22 |
00811478010008 - CAP W/AG/AGCL ELECTRODES | 2018-07-06 |
00811478010015 - SPECIAL CAP | 2018-07-06 |