Duns Number:830016148
Device Description: 3M(TM) Transpore(TM) White Tape 1534-0
Catalog Number
1534-0
Brand Name
3M™ Transpore™
Version/Model Number
1534-0
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
-
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
KGX
Product Code Name
Tape and bandage, adhesive
Public Device Record Key
4744ea2d-9311-4808-bf96-16632accb730
Public Version Date
October 23, 2019
Public Version Number
2
DI Record Publish Date
September 24, 2018
Package DI Number
50707387525915
Quantity per Package
10
Contains DI Package
30707387525911
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 |