Duns Number:118380146
Device Description: Transpac™ IV Trifurcated 60" Monitoring Kit w/3 03 ml Squeeze Flush Device and 3 Disposabl Transpac™ IV Trifurcated 60" Monitoring Kit w/3 03 ml Squeeze Flush Device and 3 Disposable Transducers
Catalog Number
46110-83
Brand Name
ICU Medical
Version/Model Number
46110-83
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K061573,K061573
Product Code
DRS
Product Code Name
Transducer, blood-pressure, extravascular
Public Device Record Key
86ea66cd-9cd8-4c79-b87d-6332d6b97896
Public Version Date
October 27, 2021
Public Version Number
1
DI Record Publish Date
October 19, 2021
Package DI Number
10840619070615
Quantity per Package
10
Contains DI Package
00840619070618
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CS
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 4887 |