Hybernite RT - Plastiflex Group NV

Duns Number:371165452

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More Product Details

Catalog Number

-

Brand Name

Hybernite RT

Version/Model Number

Hybernite RT 19 ex

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

BZE

Product Code Name

Heater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer

Device Record Status

Public Device Record Key

643f6b72-a8fc-4328-a2a5-ef254f5b4437

Public Version Date

October 24, 2022

Public Version Number

6

DI Record Publish Date

September 15, 2016

Additional Identifiers

Package DI Number

15404013000279

Quantity per Package

40

Contains DI Package

05404013000272

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"PLASTIFLEX GROUP NV" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 7
2 A medical device with a moderate to high risk that requires special controls. 17