Duns Number:002348191
Device Description: CATHETER PKGD: THERMISTOR 7,5 FR X 110 CM
Catalog Number
AI-07077-PU
Brand Name
ARROW
Version/Model Number
IPN036080
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)
Yes
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
K833918,K833918
Product Code
DYG
Product Code Name
CATHETER, FLOW DIRECTED
Public Device Record Key
e24ccf26-5fe0-41c9-821e-5c8ff2dcf73f
Public Version Date
March 10, 2021
Public Version Number
9
DI Record Publish Date
September 16, 2016
Package DI Number
60801902030643
Quantity per Package
5
Contains DI Package
00801902030641
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 | 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 |