Omnistream - Omnistream XXXX - ORIDION MEDICAL 1987 LTD.

Duns Number:600111512

Device Description: Omnistream XXXX

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More Product Details

Catalog Number

007643

Brand Name

Omnistream

Version/Model Number

007643

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"

-

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

K012395,K012395

Product Code Details

Product Code

CCK

Product Code Name

ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE

Device Record Status

Public Device Record Key

73d0ba7a-b559-42d1-aa9f-b54c04b990dc

Public Version Date

March 22, 2022

Public Version Number

4

DI Record Publish Date

November 09, 2017

Additional Identifiers

Package DI Number

20884521551753

Quantity per Package

25

Contains DI Package

10884521551756

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE

"ORIDION MEDICAL 1987 LTD." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1
2 A medical device with a moderate to high risk that requires special controls. 154