Duns Number:030849173
Device Description: ECLIPSE MALLEUS PISTON MODIFIED LOOP 0.6MM DIA X 8.00MM L NITINOL/FLUOROPLASTIC
Catalog Number
-
Brand Name
ECLIPSE MALLEUS PISTON MODIFIED LOOP
Version/Model Number
443-800
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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
K063374
Product Code
ETB
Product Code Name
Prosthesis, Partial Ossicular Replacement
Public Device Record Key
8369b0e1-75c9-4c4b-aa06-d7250f4fe77b
Public Version Date
May 18, 2020
Public Version Number
4
DI Record Publish Date
January 19, 2017
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 | 200 |
2 | A medical device with a moderate to high risk that requires special controls. | 564 |