Duns Number:187129135
Device Description: Trocar
Catalog Number
-
Brand Name
Kii Fios First Entry
Version/Model Number
CFI33
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
July 13, 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
GCJ
Product Code Name
Laparoscope, General & Plastic Surgery
Public Device Record Key
3795f605-bd9a-4ab5-8a1a-42c09593e0db
Public Version Date
January 09, 2020
Public Version Number
4
DI Record Publish Date
July 13, 2017
Package DI Number
10607915110069
Quantity per Package
6
Contains DI Package
00607915110062
Package Discontinue Date
November 02, 2016
Package Status
Not in Commercial Distribution
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 |