Trilogy Evo - Trilogy Evo O2, Eastern Europe - Respironics, Inc.

Duns Number:080728314

Device Description: Trilogy Evo O2, Eastern Europe

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More Product Details

Catalog Number

EE2100X15B

Brand Name

Trilogy Evo

Version/Model Number

EE2100X15B

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"

Yes

For Single-Use

-

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

CBK

Product Code Name

Ventilator, continuous, facility use

Device Record Status

Public Device Record Key

a7402eb2-eb77-4b53-bd8f-4b5e7d64e2d8

Public Version Date

July 06, 2020

Public Version Number

1

DI Record Publish Date

June 26, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"RESPIRONICS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 151
2 A medical device with a moderate to high risk that requires special controls. 3279