Duns Number:835233107
Device Description: ADAPTER, 9660246, PATIENT TRACKER RADIOL
Catalog Number
-
Brand Name
N/A
Version/Model Number
9660246
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 06, 2019
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
HAW
Product Code Name
Neurological stereotaxic Instrument
Public Device Record Key
90c36104-35ac-4dcc-9f76-bcdf78322f63
Public Version Date
October 18, 2021
Public Version Number
3
DI Record Publish Date
June 18, 2016
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 | 23 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1961 |
| 3 | A medical device with high risk that requires premarket approval | 1 |