Duns Number:040729840
Device Description: Castroviejo Keratoplasty and Keratectomy Scissors Wide Serrated Handle Curved Serrated Bla Castroviejo Keratoplasty and Keratectomy Scissors Wide Serrated Handle Curved Serrated Blades
Catalog Number
-
Brand Name
Castroviejo Keratoplasty and Keratectomy Scissors
Version/Model Number
13-3162
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"
Yes
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
a9a1a03b-ac65-4f2c-b354-3558917893b5
Public Version Date
January 10, 2022
Public Version Number
1
DI Record Publish Date
December 31, 2021
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 | 10108 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 3414 |