Duns Number:315018218
Device Description: T-BAR CLIP STD.PERM.JAWS 9MM KONVEX
Catalog Number
FE858K
Brand Name
AESCULAP
Version/Model Number
FE858K
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
April 19, 2017
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
HCH
Product Code Name
CLIP, ANEURYSM
Public Device Record Key
581295a8-cb66-46d2-892e-929f550bf1cc
Public Version Date
February 05, 2021
Public Version Number
5
DI Record Publish Date
September 24, 2015
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 11840 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 7088 |
| 3 | A medical device with high risk that requires premarket approval | 37 |