Duns Number:002348191
Device Description: MAC(TM) Two-Lumen Central Venous Access Super Kit with ARROWg+ard Blue(R) Access Device an MAC(TM) Two-Lumen Central Venous Access Super Kit with ARROWg+ard Blue(R) Access Device and Integral Hemostasis Valve for use with 7 - 8 Fr. Catheters
Catalog Number
AK-21142-SK
Brand Name
ARROW
Version/Model Number
IPN033954
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K011761,K011761
Product Code
DYB
Product Code Name
INTRODUCER, CATHETER
Public Device Record Key
63114fd1-f95d-4480-9052-58e882d61ba0
Public Version Date
June 07, 2019
Public Version Number
4
DI Record Publish Date
September 01, 2017
Package DI Number
10801902031201
Quantity per Package
10
Contains DI Package
20801902031208
Package Discontinue Date
May 14, 2018
Package Status
Not 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 | 3195 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 13747 |
| 3 | A medical device with high risk that requires premarket approval | 3 |
| U | Unclassified | 26 |