Poise - Sample pack containing one of each: 1) One by - KIMBERLY-CLARK GLOBAL SALES, INC.

Duns Number:829568273

Device Description: Sample pack containing one of each: 1) One by Poise Extra Coverage Liner,2) One by Poise H Sample pack containing one of each: 1) One by Poise Extra Coverage Liner,2) One by Poise Heavy Pad, 3) One by Poise Reg Pad

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More Product Details

Catalog Number

-

Brand Name

Poise

Version/Model Number

Pad

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

HHD

Product Code Name

Pad, menstrual, unscented

Device Record Status

Public Device Record Key

9a38ca3c-863e-412a-82b7-7df936aa062b

Public Version Date

April 12, 2021

Public Version Number

1

DI Record Publish Date

April 02, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"KIMBERLY-CLARK GLOBAL SALES, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 28
2 A medical device with a moderate to high risk that requires special controls. 141