Duns Number:085668598
Device Description: BARRON VACUUM PUNCH 9.0MM
Catalog Number
K20-2112
Brand Name
Corneal Trephine
Version/Model Number
K20-2112
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
HRH
Product Code Name
Trephine, manual, ophthalmic
Public Device Record Key
78e9e905-66c0-4dd5-9f4f-e6f5b92fbf9e
Public Version Date
September 22, 2020
Public Version Number
1
DI Record Publish Date
September 14, 2020
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 | 1518 |
2 | A medical device with a moderate to high risk that requires special controls. | 26 |
U | Unclassified | 63 |