Pure Comfort Adult Inhaler Spacer Chamber 4418

GUDID 10850027494415

Inaher Space Chamber with mask

HOME AIDE DIAGNOSTICS, INC.

Medicine chamber spacer, reusable
Primary Device ID10850027494415
NIH Device Record Key80321853-c1e6-4fe0-a2ed-0946840f6433
Commercial Distribution StatusIn Commercial Distribution
Brand NamePure Comfort Adult Inhaler Spacer Chamber
Version Model Number1
Catalog Number4418
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone1-800-915-0116
Emailinfo@homeaide.us
Phone1-800-915-0116
Emailinfo@homeaide.us
Phone1-800-915-0116
Emailinfo@homeaide.us
Phone1-800-915-0116
Emailinfo@homeaide.us
Phone1-800-915-0116
Emailinfo@homeaide.us
Phone1-800-915-0116
Emailinfo@homeaide.us
Phone1-800-915-0116
Emailinfo@homeaide.us
Phone1-800-915-0116
Emailinfo@homeaide.us
Phone1-800-915-0116
Emailinfo@homeaide.us
Phone1-800-915-0116
Emailinfo@homeaide.us
Phone1-800-915-0116
Emailinfo@homeaide.us
Phone1-800-915-0116
Emailinfo@homeaide.us

Device Identifiers

Device Issuing AgencyDevice ID
GS100850027494418 [Primary]
GS110850027494415 [Package]
Contains: 00850027494418
Package: Outer Case [50 Units]
In Commercial Distribution

FDA Product Code

BYPMouthpiece, Breathing

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-08-17
Device Publish Date2022-08-09

Devices Manufactured by HOME AIDE DIAGNOSTICS, INC.

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