V.A.C. VERAT.R.A.C. DUO™ - Vac Veratrac Duo Tube Set - KCI USA, INC.

Duns Number:102726734

Device Description: Vac Veratrac Duo Tube Set

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More Product Details

Catalog Number

-

Brand Name

V.A.C. VERAT.R.A.C. DUO™

Version/Model Number

ULTDUO0500

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

MR Conditional

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

K100657,K100657

Product Code Details

Product Code

OMP

Product Code Name

Negative Pressure Wound Therapy Powered Suction Pump

Device Record Status

Public Device Record Key

825515fb-8ab2-42e1-bdad-a78a4be558b6

Public Version Date

September 09, 2020

Public Version Number

5

DI Record Publish Date

September 05, 2016

Additional Identifiers

Package DI Number

00849554000162

Quantity per Package

5

Contains DI Package

00849554001374

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

5 PACK

"KCI USA, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 3
2 A medical device with a moderate to high risk that requires special controls. 63