Duns Number:187129135
Device Description: Kit Contains: CA500, EPIX® UNIVERSAL CLIP APPLIER 3/BXCTS02, 5x100 Kii® SLEEVE ZTHR 12/BXC Kit Contains: CA500, EPIX® UNIVERSAL CLIP APPLIER 3/BXCTS02, 5x100 Kii® SLEEVE ZTHR 12/BXCD001, 10mm RETRIEVAL SYSTEM, 10/BXC0R47, 12x100 Kii® BALLOON BLUNT TIP 6/BXCTB03, 5x100 Kii® SH BLD ZTHR 6/BXCB030, 5mmx35cm EPIX® LAPA SCISSOR, 10/BXC4120, 38CM GRASPER REPOS CART, 10/BX
Catalog Number
-
Brand Name
DR. J. WALKER
Version/Model Number
K2785
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"
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
FZP
Product Code Name
Clip, Implantable
Public Device Record Key
3ab6798b-6715-4fde-a36e-a602be6013c1
Public Version Date
February 05, 2021
Public Version Number
5
DI Record Publish Date
October 16, 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 | 499 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 698 |
| 3 | A medical device with high risk that requires premarket approval | 1 |