Duns Number:796986144
Device Description: LEAD 3986A60 RESUME TL IN-LINE 60CM ID
Catalog Number
-
Brand Name
RESUME® TL
Version/Model Number
3986A60
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
P840001
Product Code
GZF
Product Code Name
STIMULATOR, PERIPHERAL NERVE, IMPLANTED (PAIN RELIEF)
Public Device Record Key
79c06c7a-8365-4609-935d-2cdab26eca5f
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 23, 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 |