Catalog Number

HCB102

Brand Name

NU-DERM®

Version/Model Number

HCB102

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NAD

Product Code Name

Dressing, Wound, Occlusive

Public Device Record Key

5fd99727-e5a0-4440-86d2-b27f3af16e03

Public Version Date

July 22, 2021

Public Version Number

4

DI Record Publish Date

September 24, 2019

Package DI Number

25051978002540

Quantity per Package

20

Contains DI Package

15051978002543

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-