Dr. Scholl's

GUDID 20042825634026

Graduated Compression Support Sock for Women Moderate Support (15-20 mmHg) Knee Length, Closed Toe

RENFRO CORPORATION

Compression/pressure sock/stocking, reusable
Primary Device ID20042825634026
NIH Device Record Keye12e4796-55b9-4ee0-af7c-b53350c07666
Commercial Distribution StatusIn Commercial Distribution
Brand NameDr. Scholl's
Version Model NumberDSL-7120-BL1-SK
Company DUNS003219318
Company NameRENFRO CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone855-655-8134
Emailcallcenter@renfro.com
Phone855-655-8134
Emailcallcenter@renfro.com
Phone855-655-8134
Emailcallcenter@renfro.com
Phone855-655-8134
Emailcallcenter@renfro.com
Phone855-655-8134
Emailcallcenter@renfro.com
Phone855-655-8134
Emailcallcenter@renfro.com
Phone855-655-8134
Emailcallcenter@renfro.com
Phone855-655-8134
Emailcallcenter@renfro.com
Phone855-655-8134
Emailcallcenter@renfro.com
Phone855-655-8134
Emailcallcenter@renfro.com
Phone855-655-8134
Emailcallcenter@renfro.com
Phone855-655-8134
Emailcallcenter@renfro.com
Phone855-655-8134
Emailcallcenter@renfro.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100042825634022 [Primary]
GS120042825634026 [Package]
Contains: 00042825634022
Package: Case [12 Units]
In Commercial Distribution

FDA Product Code

DWLStocking, Medical Support (To Prevent Pooling Of Blood In Legs)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-10-07
Device Publish Date2017-08-08