Catalog Number

SNS5001G

Brand Name

Simpurity

Version/Model Number

SNS5001G

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

-

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

-

FDA Premarket Submission

-

Product Code

KOZ

Product Code Name

Beads, Hydrophilic, For Wound Exudate Absorption

Public Device Record Key

f2e868d8-58c5-4f4d-9a54-3b625286d297

Public Version Date

December 01, 2021

Public Version Number

3

DI Record Publish Date

August 12, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-