Duns Number:187129135
Device Description: Kit Contains:CA090, DIRECT DRIVE LCA 3/BXCTR33, 11X100 Kii OPT ZTHR 6/BXCTS12, 11x100 Kii Kit Contains:CA090, DIRECT DRIVE LCA 3/BXCTR33, 11X100 Kii OPT ZTHR 6/BXCTS12, 11x100 Kii SLEEVE ZTHR 12/BXCTR03, 5x100 Kii OPT ZTHR 6/BXCTS02, 5x100 Kii SLEEVE ZTHR 12/BXCD001, 10mm RETRIEVAL SYSTEM, 10/BXC2201, 120MM INSUFF NEEDLE XE, 20/BX
Catalog Number
-
Brand Name
LAP CHOLE PROCEDURE PACK
Version/Model Number
GK128
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 12, 2018
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
4affadb0-55c8-40ff-803c-031541df884e
Public Version Date
February 05, 2021
Public Version Number
5
DI Record Publish Date
October 09, 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 |