ELECTRO-GEL 32oz E10

GUDID 00811478011890

ELECTRO-CAP INTERNATIONAL INC

Electrode conductive medium
Primary Device ID00811478011890
NIH Device Record Key27a88aff-0a41-4917-8d45-de61e4f89feb
Commercial Distribution StatusIn Commercial Distribution
Brand NameELECTRO-GEL 32oz
Version Model NumberE10
Catalog NumberE10
Company DUNS186765806
Company NameELECTRO-CAP INTERNATIONAL INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone8005272193
Emaileci@electro-cap.com
Phone8005272193
Emaileci@electro-cap.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100811478011890 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GYBMedia, Electroconductive

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-10-22
Device Publish Date2016-09-23

Devices Manufactured by ELECTRO-CAP INTERNATIONAL INC

00811478010213 - NEEDLE/SYRINGE KIT - LARGE2020-12-16
00811478011883 - ELECTRO-GEL 16oz2018-10-22
00811478011890 - ELECTRO-GEL 32oz2018-10-22
00811478011890 - ELECTRO-GEL 32oz2018-10-22
00811478011906 - ELECTRO-GEL 128OZ2018-10-22
00811478011913 - ELECTRO-GEL 16OZ. BOXED2018-10-22
00811478011920 - ELECTRO-GEL 32 OZ. BOXED2018-10-22
00811478010008 - CAP W/AG/AGCL ELECTRODES2018-07-06
00811478010015 - SPECIAL CAP2018-07-06

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.