Duns Number:963383778
Device Description: SPRINT Extensa, Shipping Configuration
Catalog Number
9600-9288
Brand Name
SPRINT
Version/Model Number
Extensa, Shipping Configuration
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
-
Product Code
NHI
Product Code Name
Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief
Public Device Record Key
0248b2b0-6bc4-485c-a7b1-64fe802845a0
Public Version Date
January 08, 2021
Public Version Number
3
DI Record Publish Date
September 14, 2018
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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 85 |