Duns Number:025460908
Device Description: C-SECTION PACK 2ND-LF
Catalog Number
DYNJ17015M
Brand Name
Medline Industries, Inc.
Version/Model Number
DYNJ17015M
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
OHM
Product Code Name
Cesarean section tray
Public Device Record Key
f9582871-3117-49f0-8f72-99b9f5d015b6
Public Version Date
June 17, 2022
Public Version Number
5
DI Record Publish Date
August 28, 2018
Package DI Number
40889942778776
Quantity per Package
3
Contains DI Package
10889942778775
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 |