Duns Number:025460908
Device Description: DRAPE CYSTO LARGE
Catalog Number
DYNJP5002
Brand Name
MEDLINE INDUSTRIES, INC.
Version/Model Number
DYNJP5002
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
KKX
Product Code Name
Drape, surgical
Public Device Record Key
99a7fa30-ff8b-4e6a-905e-fcdf44d44f7e
Public Version Date
December 22, 2021
Public Version Number
3
DI Record Publish Date
December 31, 2020
Package DI Number
40884389192123
Quantity per Package
12
Contains DI Package
10884389192122
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 |