Duns Number:192135242
Device Description: PMI IV START KIT W/ PVP LATEX FREE
Catalog Number
K703
Brand Name
PMI
Version/Model Number
K703
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
-
Product Code Name
-
Public Device Record Key
2058b7f9-37d8-4c08-8b1b-e07bc02f63a6
Public Version Date
December 11, 2019
Public Version Number
3
DI Record Publish Date
September 19, 2016
Package DI Number
00812608021390
Quantity per Package
50
Contains DI Package
00812608021383
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 | 23 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 112 |