Duns Number:315620229
Catalog Number
118718
Brand Name
DF1-C6HV
Version/Model Number
118718
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 27, 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
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
P980023
Product Code
DTD
Product Code Name
pacemaker lead Adaptor
Public Device Record Key
7d4ab976-9d60-4490-8be1-96289d74caee
Public Version Date
August 30, 2021
Public Version Number
5
DI Record Publish Date
August 25, 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 | 1 |
2 | A medical device with a moderate to high risk that requires special controls. | 97 |
3 | A medical device with high risk that requires premarket approval | 402 |