Duns Number:360624720
Device Description: MaxGuard multi-fuse extension set with needleless connector (s)
Catalog Number
MP9208
Brand Name
MaxPlus, MaxGuard
Version/Model Number
MP9208
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
FPA
Product Code Name
Set, administration, intravascular
Public Device Record Key
b7066204-f435-4588-aa85-f6bc3db4d75f
Public Version Date
April 27, 2020
Public Version Number
4
DI Record Publish Date
November 04, 2016
Package DI Number
20885403428026
Quantity per Package
12
Contains DI Package
50885403428027
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 2 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 43 |