Duns Number:002348191
Device Description: Epidural Catheterization Kit with FlexTip Plus(R) Catheter FOR EXPORT ONLY
Catalog Number
ASK-05500-KM
Brand Name
ARROW
Version/Model Number
IPN042606
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
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
OGE
Product Code Name
Epidural anesthesia kit
Public Device Record Key
1401641f-7abe-4114-82c2-eb8d2496b03a
Public Version Date
November 08, 2019
Public Version Number
3
DI Record Publish Date
March 02, 2018
Package DI Number
40801902128155
Quantity per Package
5
Contains DI Package
30801902128158
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 | 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 |