Duns Number:006261481
Device Description: MON 24950J MYCARELINK/SVC USA
Catalog Number
-
Brand Name
MyCareLink™
Version/Model Number
24950J
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
P890003,P890003,P890003,P890003
Product Code
NVZ
Product Code Name
Pulse generator, permanent, implantable
Public Device Record Key
6e6f10ca-0478-41a6-8bd2-e78bf4adcd2b
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
December 18, 2015
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 | 102 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 20495 |
| 3 | A medical device with high risk that requires premarket approval | 3601 |