Catalog Number

1668

Brand Name

3M™ Tegaderm™

Version/Model Number

1668

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

NAD

Product Code Name

Dressing, wound, occlusive

Public Device Record Key

45c3cab0-e6d5-402d-9a1a-ec0805e7d2bc

Public Version Date

December 22, 2021

Public Version Number

2

DI Record Publish Date

September 24, 2018

Package DI Number

50707387770384

Quantity per Package

4

Contains DI Package

30707387770380

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX