Duns Number:020163218
Catalog Number
D7TCEG252RT
Brand Name
Celsius
Version/Model Number
D7TCEG252RT
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
March 19, 2019
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
P950005
Product Code
LPB
Product Code Name
Cardiac ablation percutaneous catheter
Public Device Record Key
6a5af001-fca1-498d-bd2a-2bf777e9d674
Public Version Date
June 07, 2022
Public Version Number
6
DI Record Publish Date
September 10, 2014
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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 354 |
3 | A medical device with high risk that requires premarket approval | 183 |