3M™ Tegaderm™ - 3M(TM) Tegaderm(TM) Transparent Film Dressing - 3M COMPANY

Duns Number:830016148

Device Description: 3M(TM) Tegaderm(TM) Transparent Film Dressing Frame Style 1622W

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More Product Details

Catalog Number

1622W

Brand Name

3M™ Tegaderm™

Version/Model Number

1622W

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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 Details

Product Code

NAD

Product Code Name

Dressing, wound, occlusive

Device Record Status

Public Device Record Key

d7a3b21c-5420-4a95-a14d-98b7955a27fb

Public Version Date

December 22, 2021

Public Version Number

2

DI Record Publish Date

September 24, 2018

Additional Identifiers

Package DI Number

50707387509472

Quantity per Package

4

Contains DI Package

04001895928673

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX

"3M COMPANY" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 274
2 A medical device with a moderate to high risk that requires special controls. 444
U Unclassified 7