Duns Number:021717889
Device Description: Guidewire
Catalog Number
-
Brand Name
Zebra
Version/Model Number
M0066701130
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
EZB
Product Code Name
STYLET FOR CATHETER, GASTRO-UROLOGY
Public Device Record Key
cf2ac1b7-b882-40a8-9e5c-d54ce814fa10
Public Version Date
November 15, 2018
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
08714729191261
Quantity per Package
5
Contains DI Package
08714729516392
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 536 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 8659 |
| 3 | A medical device with high risk that requires premarket approval | 1821 |
| U | Unclassified | 35 |