Duns Number:695221077
Catalog Number
-
Brand Name
ECLIPSE Ti2-U IVF US
Version/Model Number
MEA54500
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
MTX
Product Code Name
Microscope And Microscope Accessories, Reproduction, Assisted
Public Device Record Key
ef8ae848-8445-4cf7-a290-0e74f468a0f7
Public Version Date
August 31, 2021
Public Version Number
1
DI Record Publish Date
August 23, 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 | 1 |