Duns Number:071595540
Device Description: Multiple Use Titanium Cannula
Catalog Number
RC-11R
Brand Name
ONEPORT
Version/Model Number
RC-11R
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 07, 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
-
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
K073009,K073009
Product Code
GCJ
Product Code Name
Laparoscope, general & plastic surgery
Public Device Record Key
42e061ac-ea86-4c39-b48a-6b03754ee777
Public Version Date
June 08, 2022
Public Version Number
4
DI Record Publish Date
September 24, 2016
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 | 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 |