GUDID 20840682102814

GE Healthcare Finland Oy

Breathing circuit condensate trap, reusable
Primary Device ID20840682102814
NIH Device Record Keyd2f96782-bd38-41e8-90da-1d2414db2ab2
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberD-fend Water Trap, 881319-HEL
Company DUNS401966697
Company NameGE Healthcare Finland Oy
Device Count1
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100840682102810 [Primary]
GS120840682102814 [Package]
Contains: 00840682102810
Package: [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHOAnalyzer, gas, desflurane, gaseous-phase (anesthetic concentration)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-08-15

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