INTEGRA® VolTAC™ - Integra VolTAC Antimicrobial Wound Dressing is a - Integra Lifesciences Corporation

Duns Number:083171244

Device Description: Integra VolTAC Antimicrobial Wound Dressing is a single layer dressing. VolTAC consists of Integra VolTAC Antimicrobial Wound Dressing is a single layer dressing. VolTAC consists of a polyester substrate containing elemental silver and zinc applied on the surface in a dot-matrix pattern. In the presence of a conductive medium (e.g. wound exudate, water-based wound hydrogel, sterile saline or sterile water), silver and zinc in the dressing generate microcurrents at the dressing surface which helps preserve the dressing and minimizes or prevents the growth of microorganisms within the dressing.

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More Product Details

Catalog Number

-

Brand Name

INTEGRA® VolTAC™

Version/Model Number

VOLS0205

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K130350,K130350

Product Code Details

Product Code

FRO

Product Code Name

Dressing, wound, drug

Device Record Status

Public Device Record Key

f62e0ab1-920a-402b-84ea-c7ffb811dce4

Public Version Date

September 22, 2020

Public Version Number

4

DI Record Publish Date

July 21, 2016

Additional Identifiers

Package DI Number

30381780257879

Quantity per Package

10

Contains DI Package

10381780257875

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX

"INTEGRA LIFESCIENCES CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 14
2 A medical device with a moderate to high risk that requires special controls. 75
3 A medical device with high risk that requires premarket approval 17
U Unclassified 32