Duns Number:831375089
Device Description: Pressure Infusion Bag, Reusable, 500mL, Clear Back
Catalog Number
8817
Brand Name
PremierPro
Version/Model Number
8817
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)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
KZD
Product Code Name
Infusor, Pressure, For I.V. Bags
Public Device Record Key
3f53be08-4704-4de7-b855-6b628b5f7ad2
Public Version Date
November 19, 2020
Public Version Number
2
DI Record Publish Date
August 29, 2020
Package DI Number
10811220030046
Quantity per Package
20
Contains DI Package
00811220030049
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 | 486 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 177 |
| U | Unclassified | 1 |