Venner™ PneuX P.Y.™ ETT 901080

GUDID 08885009190738

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 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 ID08885009190738
NIH Device Record Key2be236dc-28fd-4ab8-857e-e1babd75f789
Commercial Distribution StatusIn Commercial Distribution
Brand NameVenner™ PneuX P.Y.™ ETT
Version Model Number901080
Catalog Number901080
Company DUNS659177273
Company NameVENNER MEDICAL (SINGAPORE) PTE. LTD.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
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 Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter
Lumen/Inner Diameter8 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS108885009190738 [Primary]
GS118885009190735 [Package]
Package: 10 pouches in a box [10 Units]
In Commercial Distribution
GS128885009190732 [Package]
Contains: 18885009190735
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]

08885009190745The Venner™ PneuX P.Y.™ Endotracheal tube is designed to be used for patients undergoing Tra
08885009190738The Venner™ PneuX P.Y.™ Endotracheal tube is designed to be used for patients undergoing Tra
08885009190721The Venner™ PneuX P.Y.™ Endotracheal tube is designed to be used for patients undergoing Tra
08885009190714The 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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