MC300® Nebulizer with Corrugated Tubing, Mouthpiece and Universal Tubing 10555794050

GUDID 10762860055572

MC300® Nebulizer with Corrugated Tubing, Mouthpiece and Universal Tubing

Trudell Medical International

Nebulizing system delivery set, reusable
Primary Device ID10762860055572
NIH Device Record Key998b7571-1368-4f79-99f3-77ab4696d038
Commercial Distribution StatusIn Commercial Distribution
Brand NameMC300® Nebulizer with Corrugated Tubing, Mouthpiece and Universal Tubing
Version Model Number105557
Catalog Number10555794050
Company DUNS203298203
Company NameTrudell Medical International
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-519-455-4862
Emailcustomerservice@trudellmed.com
Phone1-519-455-4862
Emailcustomerservice@trudellmed.com
Phone1-519-455-4862
Emailcustomerservice@trudellmed.com
Phone1-519-455-4862
Emailcustomerservice@trudellmed.com
Phone1-519-455-4862
Emailcustomerservice@trudellmed.com
Phone1-519-455-4862
Emailcustomerservice@trudellmed.com
Phone1-519-455-4862
Emailcustomerservice@trudellmed.com
Phone1-519-455-4862
Emailcustomerservice@trudellmed.com
Phone1-519-455-4862
Emailcustomerservice@trudellmed.com
Phone1-519-455-4862
Emailcustomerservice@trudellmed.com
Phone1-519-455-4862
Emailcustomerservice@trudellmed.com
Phone1-519-455-4862
Emailcustomerservice@trudellmed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100762860055575 [Primary]
GS110762860055572 [Package]
Contains: 00762860055575
Package: [50 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

CAFNebulizer (Direct Patient Interface)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-29
Device Publish Date2021-06-21

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