Resp-O2 Heat Moisture Exchanger - Resp-O2 Heat Moisture Exchanger (HME) 1500, - DYNAREX CORPORATION

Duns Number:008124539

Device Description: Resp-O2 Heat Moisture Exchanger (HME) 1500, Integrated Flex Tube; Adult/Ped

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More Product Details

Catalog Number

-

Brand Name

Resp-O2 Heat Moisture Exchanger

Version/Model Number

30202

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

MR Safe

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"

Yes

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

K132709,K132709

Product Code Details

Product Code

CAH

Product Code Name

Filter, Bacterial, Breathing-Circuit

Device Record Status

Public Device Record Key

095bff03-e8f3-4fd7-b87b-9f7f101145fb

Public Version Date

January 31, 2022

Public Version Number

2

DI Record Publish Date

April 22, 2021

Additional Identifiers

Package DI Number

00840117318083

Quantity per Package

50

Contains DI Package

00840117318090

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case

"DYNAREX CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 694
2 A medical device with a moderate to high risk that requires special controls. 226
3 A medical device with high risk that requires premarket approval 2