Duns Number:175899459
Device Description: EP DIAGNOSTIC CATHETER DECAPOLAR D-TYPE/BLUE
Catalog Number
BIOD6-10DR-252-RT-DP
Brand Name
NA
Version/Model Number
BIOD6-10DR-252-RT-DP
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
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
K043513
Product Code
NLH
Product Code Name
CATHETER, RECORDING, ELECTRODE, REPROCESSED
Public Device Record Key
b4258b4f-1fa8-4f63-a865-71fc56890b4e
Public Version Date
August 14, 2019
Public Version Number
4
DI Record Publish Date
September 22, 2016
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 | 2763 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1372 |
| U | Unclassified | 20 |