3M™ Veraflo™ Cleanse Choice Complete™ - 3M™ Veraflo™ Cleanse Choice Complete™ Dressing - KCI USA, INC.

Duns Number:102726734

Device Description: 3M™ Veraflo™ Cleanse Choice Complete™ Dressing Kit Large

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More Product Details

Catalog Number

VFCCC05LG

Brand Name

3M™ Veraflo™ Cleanse Choice Complete™

Version/Model Number

VFCCC05LG

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

MR Safe

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

-

Product Code Details

Product Code

OMP

Product Code Name

negative pressure wound therapy Powered suction pump

Device Record Status

Public Device Record Key

830ffd21-2cef-49c6-b77b-d5db82a249b8

Public Version Date

January 21, 2022

Public Version Number

1

DI Record Publish Date

January 13, 2022

Additional Identifiers

Package DI Number

00849554008182

Quantity per Package

5

Contains DI Package

00849554008151

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX

"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