Catalog Number
DYNDA2428
Brand Name
MEDLINE
Version/Model Number
DYNDA2428
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
KXG
Product Code Name
APPLICATOR, ABSORBENT TIPPED, STERILE
Public Device Record Key
9a07f6da-b6c9-4c0e-be87-caf922bd4bf8
Public Version Date
January 08, 2021
Public Version Number
2
DI Record Publish Date
May 11, 2020
Package DI Number
20888277732923
Quantity per Package
50
Contains DI Package
10888277732926
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 |