BIOPATCH - BioPatch™ Antimicrobial Dressing with - ETHICON INC.

Duns Number:002144145

Device Description: BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyuretha BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms.

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

10151

Brand Name

BIOPATCH

Version/Model Number

10151

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

Yes

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K003229,K003229,K003229

Product Code Details

Product Code

FRO

Product Code Name

Dressing, wound, drug

Device Record Status

Public Device Record Key

3f7792bb-fdfb-4e0c-bdf8-a93f303bae3d

Public Version Date

July 08, 2021

Public Version Number

10

DI Record Publish Date

June 20, 2016

Additional Identifiers

Package DI Number

30705031001118

Quantity per Package

500

Contains DI Package

10705031001114

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE

"ETHICON INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 29
2 A medical device with a moderate to high risk that requires special controls. 1128
3 A medical device with high risk that requires premarket approval 4
U Unclassified 1