Duns Number:071595540
Device Description: CLEARVAC GOLDLINE FOOT CONTROLLED WITH ULTRACLEAN BLADE ELECTRODE ELECTROSURGICAL HANDPIEC CLEARVAC GOLDLINE FOOT CONTROLLED WITH ULTRACLEAN BLADE ELECTRODE ELECTROSURGICAL HANDPIECE
Catalog Number
138663A
Brand Name
CLEARVAC GOLDLINE
Version/Model Number
138663A
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"
-
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
GEI
Product Code Name
ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
Public Device Record Key
7f176f90-2061-4ffd-842f-4d78b4567ee6
Public Version Date
February 07, 2019
Public Version Number
3
DI Record Publish Date
July 13, 2017
Package DI Number
20653405056406
Quantity per Package
10
Contains DI Package
10653405056409
Package Discontinue Date
-
Package Status
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 |