BIONIX DEVELOPMENT CORPORATION - Sample-DeClogger 14-16 F/Brown - BIONIX DEVELOPMENT CORPORATION

Duns Number:602736795

Device Description: Sample-DeClogger 14-16 F/Brown

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More Product Details

Catalog Number

921

Brand Name

BIONIX DEVELOPMENT CORPORATION

Version/Model Number

SP-20921

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

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

K905164

Product Code Details

Product Code

KNT

Product Code Name

TUBES, GASTROINTESTINAL (AND ACCESSORIES)

Device Record Status

Public Device Record Key

ce9a4ecb-df6c-4c7a-a4b7-59b8a6d0313a

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

February 22, 2017

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"BIONIX DEVELOPMENT CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 2
2 A medical device with a moderate to high risk that requires special controls. 23