Duns Number:071595540
Device Description: 5mm Trocar And Flexible Cannula
Catalog Number
CD1730
Brand Name
CORE DYNAMICS
Version/Model Number
CD1730
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 09, 2022
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
K950457,K950457,K950457
Product Code
HET
Product Code Name
LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)
Public Device Record Key
e3278aad-8029-4369-b73e-cb079b991b92
Public Version Date
June 10, 2022
Public Version Number
5
DI Record Publish Date
September 24, 2016
Package DI Number
10653405045205
Quantity per Package
10
Contains DI Package
20653405045202
Package Discontinue Date
June 09, 2022
Package Status
Not 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 | 1412 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 2261 |
| 3 | A medical device with high risk that requires premarket approval | 95 |