Duns Number:068156330
Device Description: DISPOSABLE SUBDERMAL NEEDLE ELECTRODES: 27 GA., 6 MM NEEDLE, 2.3 M (90") TWISTED LEADWIRE, DISPOSABLE SUBDERMAL NEEDLE ELECTRODES: 27 GA., 6 MM NEEDLE, 2.3 M (90") TWISTED LEADWIRE, COLOR GROUP 1
Catalog Number
-
Brand Name
Rochester
Version/Model Number
S06666-P
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
October 24, 2016
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
44dba42d-e890-4a99-8959-3f4140391a5f
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
September 24, 2016
Package DI Number
10816843021655
Quantity per Package
10
Contains DI Package
10816843021662
Package Discontinue Date
October 24, 2016
Package Status
Not in Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 83 |