Duns Number:080242300
Device Description: DISPOSABLE SUREPOINT SUBDERMAL NEEDLE ELECTRODES: 29 GA., 13 MM NEEDLE, 0.5 M (18") SINGLE DISPOSABLE SUREPOINT SUBDERMAL NEEDLE ELECTRODES: 29 GA., 13 MM NEEDLE, 0.5 M (18") SINGLE LEADWIRE, COLOR 18P - 20 /BOX
Catalog Number
-
Brand Name
SurePoint™
Version/Model Number
NS-S02918-P-20
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
GXZ
Product Code Name
Electrode, Needle
Public Device Record Key
0eae53a4-395f-4020-91d8-6f7d2d655e70
Public Version Date
August 13, 2018
Public Version Number
1
DI Record Publish Date
July 11, 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. | 1261 |