Catalog Number

-

Brand Name

SORBALGON 4X4 10/BX

Version/Model Number

49210001

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NAC

Product Code Name

Dressing, Wound, Hydrophilic

Public Device Record Key

f813fd00-fe77-43cc-8b8b-52244006d78f

Public Version Date

July 22, 2021

Public Version Number

2

DI Record Publish Date

September 01, 2020

Package DI Number

04052199569802

Quantity per Package

10

Contains DI Package

04052199569796

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-