Duns Number:790268031
Device Description: Defibrillation Lead
Catalog Number
LDA210Q-58
Brand Name
OPTISURE™
Version/Model Number
LDA210Q-58
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
P950022,P950022,P950022,P950022,P950022
Product Code
NVY
Product Code Name
Permanent defibrillator electrodes
Public Device Record Key
08f47abe-d7ec-4e4e-8627-2ca2000c77e1
Public Version Date
February 05, 2021
Public Version Number
7
DI Record Publish Date
February 03, 2017
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 | 70 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1429 |
| 3 | A medical device with high risk that requires premarket approval | 736 |