Pure Comfort Posture Corrector

GUDID 10860006377820

Posture Corrector

HOME AIDE DIAGNOSTICS, INC.

Lumbar spine orthosis
Primary Device ID10860006377820
NIH Device Record Keyca393739-ae62-4071-9887-22f2b9119b80
Commercial Distribution StatusIn Commercial Distribution
Brand NamePure Comfort Posture Corrector
Version Model NumberPCorrector
Company DUNS783518983
Company NameHOME AIDE DIAGNOSTICS, INC.
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

Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us
Phone8009150116
Emailinfo@homeaide.us

Device Identifiers

Device Issuing AgencyDevice ID
GS100860006377823 [Primary]
GS110860006377820 [Package]
Contains: 00860006377823
Package: Outer Case [162 Units]
In Commercial Distribution

FDA Product Code

KTDOrthosis, Abdominal

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-11-13
Device Publish Date2023-11-03

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