Duns Number:595138793
Device Description: A critiflo Dome set
Catalog Number
682058
Brand Name
CRITIFLO(TM) TA1015T (3ML/HR)
Version/Model Number
682058
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
KRA
Product Code Name
Catheter, Continuous Flush
Public Device Record Key
a03368e9-8201-4156-bec6-da90f9931b3b
Public Version Date
June 11, 2018
Public Version Number
3
DI Record Publish Date
September 23, 2016
Package DI Number
50886333620581
Quantity per Package
100
Contains DI Package
00886333620586
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Tyvek Pouch
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 392 |