Duns Number:080254074
Device Description: ELEOS™ MALE-MALE MIDSECTION TRIAL, 40MM
Catalog Number
MT-00040-02N
Brand Name
ELEOS™
Version/Model Number
MT-00040-02N
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
K161520
Product Code
HWT
Product Code Name
TEMPLATE
Public Device Record Key
cc84c6fe-cf8b-42d0-a2dd-33726901cd52
Public Version Date
July 29, 2020
Public Version Number
1
DI Record Publish Date
July 21, 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 | 378 |
2 | A medical device with a moderate to high risk that requires special controls. | 231 |
3 | A medical device with high risk that requires premarket approval | 4 |