Duns Number:006261481
Device Description: MONITOR 24955 FRU US CAN ANZ EUR 1 BD
Catalog Number
-
Brand Name
MyCareLink™
Version/Model Number
24955
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
April 15, 2021
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
Product Code
OSR
Product Code Name
Pacemaker/icd/crt non-implanted components
Public Device Record Key
0ba23349-a740-4418-908f-4083770fe63b
Public Version Date
January 31, 2022
Public Version Number
4
DI Record Publish Date
October 31, 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 |
|---|---|---|
| 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 |