Duns Number:830016148
Device Description: 3M™ Tegaderm™ High Gelling Alginate Dressing, 90220, 1 in x 12 in, Rope Style Dressing, 5/ 3M™ Tegaderm™ High Gelling Alginate Dressing, 90220, 1 in x 12 in, Rope Style Dressing, 5/Carton, 4 Cartons/Case
Catalog Number
90220
Brand Name
3M™ Tegaderm™
Version/Model Number
90220
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"
-
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
NAC
Product Code Name
Dressing, wound, hydrophilic
Public Device Record Key
9cfb8ab9-484a-4a7a-b31c-58f8b9887dab
Public Version Date
July 22, 2021
Public Version Number
2
DI Record Publish Date
July 09, 2021
Package DI Number
50707387793512
Quantity per Package
4
Contains DI Package
00707387793524
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
BOX
| 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 |