Duns Number:025460908
Device Description: KIT PLASTIC ABDOMINOPLASTY
Catalog Number
DYKMBNDL170A
Brand Name
Medline Industries, Inc.
Version/Model Number
DYKMBNDL170A
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
FTN
Product Code Name
Plastic surgery and accessories kit
Public Device Record Key
feec0949-a431-40e5-9059-1f3eba50c001
Public Version Date
September 12, 2022
Public Version Number
1
DI Record Publish Date
September 04, 2022
Package DI Number
40195327240814
Quantity per Package
3
Contains DI Package
10195327240813
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 |