Catalog Number

90002

Brand Name

3M™ Tegaderm™

Version/Model Number

90002

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)

Yes

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

5cb09f98-cdf9-45c0-8afc-52538be90ea9

Public Version Date

July 22, 2021

Public Version Number

3

DI Record Publish Date

September 24, 2018

Package DI Number

50707387082067

Quantity per Package

20

Contains DI Package

05000485089618

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX