Duns Number:025460908
Device Description: CLOSURE PACK
Catalog Number
DYNJ69995
Brand Name
Medline Industries, Inc.
Version/Model Number
DYNJ69995
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
MCY
Product Code Name
Wound dressing kit
Public Device Record Key
b93f7969-affe-4a88-b42e-4bc2927bb1f5
Public Version Date
June 17, 2022
Public Version Number
2
DI Record Publish Date
October 03, 2021
Package DI Number
40195327004164
Quantity per Package
3
Contains DI Package
10195327004620
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 |