Duns Number:962519208
Device Description: Reusable Gold Disc electrode teflon leads
Catalog Number
101007-T
Brand Name
Natus
Version/Model Number
Gold Disc Electrode Teflon
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
-
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K030823,K031009,K073626,K073665,K083371,K111618,K112247,K121512,K122496,K141446,K030823,K031009,K073626,K073665,K083371,K111618,K112247,K121512,K122496,K141446
Product Code
EWO
Product Code Name
Audiometer
Public Device Record Key
97d3035e-aca1-42c7-bcae-dc08fca4415d
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
May 09, 2017
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 | 24 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 302 |
| 3 | A medical device with high risk that requires premarket approval | 5 |