ENDOTRACHEAL TUBE, WIRE REINFORCED, WITH CUFF - Endotracheal Tubes are intended for oral - FUJI SYSTEMS CORPORATION

Duns Number:715919973

Device Description: Endotracheal Tubes are intended for oral intubation and are indicated for use in airway ma Endotracheal Tubes are intended for oral intubation and are indicated for use in airway management and other suitable medical application.

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More Product Details

Catalog Number

1200824

Brand Name

ENDOTRACHEAL TUBE, WIRE REINFORCED, WITH CUFF

Version/Model Number

I.D. 5.5MM (FR.24), 400MM LONG TYPE

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)

-

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

BTR

Product Code Name

Tube, Tracheal (W/Wo Connector)

Device Record Status

Public Device Record Key

5cacadbd-c949-421a-854d-d98ca985c681

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 24, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"FUJI SYSTEMS CORPORATION" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 32