VentStar Helix heated

GUDID 04048675253372

Drägerwerk AG & Co. KGaA

Ventilator breathing circuit, single-use
Primary Device ID04048675253372
NIH Device Record Keya4eb7f5c-1d94-4473-a05e-3ebd863c529c
Commercial Distribution StatusIn Commercial Distribution
Brand NameVentStar Helix heated
Version Model NumberMP02607
Company DUNS315578914
Company NameDrägerwerk AG & Co. KGaA
Device Count10
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
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-Counterfalse

Customer Support Contacts

Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com
Phone+494518820
Emailinfo@draeger.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104048675253372 [Primary]
GS104048675420347 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

BTTHumidifier, Respiratory Gas, (Direct Patient Interface)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-11-27
Device Publish Date2015-10-24

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