Duns Number:832696038
Device Description: GILLS-WELSH-VANNAS CAPSULOTOMY SCISS, ANG BLDES, 5MM FROM MID-SCREW OVERALL LENGTH 3"(7.6C GILLS-WELSH-VANNAS CAPSULOTOMY SCISS, ANG BLDES, 5MM FROM MID-SCREW OVERALL LENGTH 3"(7.6CM)
Catalog Number
OP9303
Brand Name
V. Mueller
Version/Model Number
OP9303
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
-
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
HNF
Product Code Name
SCISSORS, OPHTHALMIC
Public Device Record Key
dca3bdaf-7682-447a-a42f-619938ac1f43
Public Version Date
September 23, 2022
Public Version Number
3
DI Record Publish Date
September 07, 2018
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 | 8016 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 6223 |