Duns Number:202981171
Device Description: Reusable Surgical Instrument Set
Catalog Number
027-003
Brand Name
BC Reflex Uni Reusable Surgical Instrument Set
Version/Model Number
027-003
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
K211646
Product Code
HSX
Product Code Name
Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
Public Device Record Key
2e8cd6c0-d57e-4f71-b391-a614ee7eb771
Public Version Date
December 22, 2021
Public Version Number
1
DI Record Publish Date
December 13, 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 | 5 |
2 | A medical device with a moderate to high risk that requires special controls. | 75 |