Duns Number:025460908
Device Description: DBD-BANDAGE,SRTSTRTCH,10CMX5M,3.94X5.47Y
Catalog Number
MDS099004SSHL
Brand Name
Medline
Version/Model Number
MDS099004SSHL
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
FQM
Product Code Name
BANDAGE, ELASTIC
Public Device Record Key
20f13528-7c8d-46a3-b85d-4ff75c4ccc16
Public Version Date
September 20, 2021
Public Version Number
2
DI Record Publish Date
January 20, 2021
Package DI Number
20888277702285
Quantity per Package
20
Contains DI Package
10888277702288
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 38540 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 85094 |
| 3 | A medical device with high risk that requires premarket approval | 2 |
| U | Unclassified | 7 |