O-Two - The O-Two single-use ventilation circuit is - O-Two Medical Technologies Inc

Duns Number:206449154

Device Description: The O-Two single-use ventilation circuit is designed to be used with ventilators, demand v The O-Two single-use ventilation circuit is designed to be used with ventilators, demand valve or gas mixers to deliver oxygen or nitrous oxide and oxygen mixture gas to patients. It consists of one corrugated breathing hose, an inspiratory one-way valve, and a PEEP port. The 01CV8016 is specifically designed for use with CAREvent MRI ventilators and is long enough to allow free passage of the patient in and out of the MRI unit without the risk of pulling on the tubing.

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More Product Details

Catalog Number

01CV8016-CS

Brand Name

O-Two

Version/Model Number

01CV8016

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

CAI

Product Code Name

Circuit, Breathing (W Connector, Adaptor, Y Piece)

Device Record Status

Public Device Record Key

26a36a84-a180-4b30-a78d-a6c3eb1a36e8

Public Version Date

October 24, 2022

Public Version Number

3

DI Record Publish Date

May 31, 2019

Additional Identifiers

Package DI Number

17540195005188

Quantity per Package

10

Contains DI Package

07540195005181

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"O-TWO MEDICAL TECHNOLOGIES INC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 32
2 A medical device with a moderate to high risk that requires special controls. 48
U Unclassified 3