Duns Number:055527753
Device Description: STACKABLE CONTAINER 5.4 QT. TRANSLUCENT RED W/LID
Catalog Number
8708T
Brand Name
Medegen Medical products
Version/Model Number
8708T
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 01, 2020
Issuing Agency
In HIBCC
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)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K942054,K942054
Product Code
FMI
Product Code Name
Needle, hypodermic, single lumen
Public Device Record Key
6fabb328-0ce4-43f5-abd0-cbd2a0db71fd
Public Version Date
June 01, 2020
Public Version Number
5
DI Record Publish Date
September 23, 2016
Package DI Number
H3628708T2
Quantity per Package
12
Contains DI Package
H3628708T0
Package Discontinue Date
June 01, 2020
Package Status
Not in Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 14 |
2 | A medical device with a moderate to high risk that requires special controls. | 108 |