RICHMAR

GUDID 00092237626290

EMG CHANNEL LEAD WIRE

COMPASS HEALTH BRANDS CORP.

Transcutaneous electrical stimulation lead Transcutaneous electrical stimulation lead Transcutaneous electrical stimulation lead Transcutaneous electrical stimulation lead Transcutaneous electrical stimulation lead Transcutaneous electrical stimulation lead Transcutaneous electrical stimulation lead Transcutaneous electrical stimulation lead Transcutaneous electrical stimulation lead Transcutaneous electrical stimulation lead Transcutaneous electrical stimulation lead Transcutaneous electrical stimulation lead
Primary Device ID00092237626290
NIH Device Record Key100592ae-fc33-4ab2-af7f-9b098697ab93
Commercial Distribution StatusIn Commercial Distribution
Brand NameRICHMAR
Version Model NumberEMG-CLW
Company DUNS827221698
Company NameCOMPASS HEALTH BRANDS CORP.
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-376-7263
Emailcustomerservice@compasshealthbrands.com
Phone800-376-7263
Emailcustomerservice@compasshealthbrands.com
Phone800-376-7263
Emailcustomerservice@compasshealthbrands.com
Phone800-376-7263
Emailcustomerservice@compasshealthbrands.com
Phone800-376-7263
Emailcustomerservice@compasshealthbrands.com
Phone800-376-7263
Emailcustomerservice@compasshealthbrands.com
Phone800-376-7263
Emailcustomerservice@compasshealthbrands.com
Phone800-376-7263
Emailcustomerservice@compasshealthbrands.com
Phone800-376-7263
Emailcustomerservice@compasshealthbrands.com
Phone800-376-7263
Emailcustomerservice@compasshealthbrands.com
Phone800-376-7263
Emailcustomerservice@compasshealthbrands.com
Phone800-376-7263
Emailcustomerservice@compasshealthbrands.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100092237626290 [Primary]

FDA Product Code

IKDCable, Electrode

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-06-05
Device Publish Date2024-05-28

On-Brand Devices [RICHMAR]

00092237626290EMG CHANNEL LEAD WIRE
00092237626283EMG REFERENCE LEAD WIRE

Trademark Results [RICHMAR]

Mark Image

Registration | Serial
Company
Trademark
Application Date
RICHMAR
RICHMAR
87164514 5181445 Live/Registered
COMPASS RICHMAR, LLC
2016-09-08
RICHMAR
RICHMAR
73026773 1043218 Dead/Expired
Richmar Products, Inc.
1974-07-15
RICHMAR
RICHMAR
73009392 1004295 Dead/Cancelled
Apeco Corporation
0000-00-00

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