Venner™ PneuX P.Y.™ ETT MRI 901170

GUDID 28885009190763

The Venner™ PneuX P.Y.™ Endotracheal tube is designed to be used for patients undergoing Tracheal intubation during extended periods (not more than 30 days) of intensive or critical care, and for evacuation or drainage of secretion from the subglottic space. It is also safety in an MRI environment (indicated MRI) and compatible with Tracheal intubation during routine anaesthesia.

VENNER MEDICAL (SINGAPORE) PTE. LTD.

Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use
Primary Device ID28885009190763
NIH Device Record Keyc84f1b7d-ddca-4dca-8fe4-72725a76e303
Commercial Distribution StatusIn Commercial Distribution
Brand NameVenner™ PneuX P.Y.™ ETT MRI
Version Model Number901170
Catalog Number901170
Company DUNS659177273
Company NameVENNER MEDICAL (SINGAPORE) PTE. LTD.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Producttrue
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 Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Dimensions

Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter
Lumen/Inner Diameter7 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS108885009190769 [Primary]
GS118885009190766 [Package]
Contains: 08885009190769
Package: 10 pouches in a box [10 Units]
In Commercial Distribution
GS128885009190763 [Package]
Contains: 18885009190766
Package: 10 boxes in a carton [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

BTRTube, Tracheal (W/Wo Connector)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-05-06
Device Publish Date2016-09-24

On-Brand Devices [Venner™ PneuX P.Y.™ ETT MRI]

28885009190787The Venner™ PneuX P.Y.™ Endotracheal tube is designed to be used for patients undergoing Tra
28885009190770The Venner™ PneuX P.Y.™ Endotracheal tube is designed to be used for patients undergoing Tra
28885009190763The Venner™ PneuX P.Y.™ Endotracheal tube is designed to be used for patients undergoing Tra
28885009190756The Venner™ PneuX P.Y.™ Endotracheal tube is designed to be used for patients undergoing Tra

Trademark Results [Venner]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VENNER
VENNER
77621249 4305467 Live/Registered
INDIAN OCEAN MEDICAL INC.
2008-11-25
VENNER
VENNER
77621241 not registered Dead/Abandoned
Venner Capital S.A.
2008-11-25

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