Duns Number:383228632
Device Description: PEDICLE PROBE
Catalog Number
-
Brand Name
PASS MIS
Version/Model Number
A06010510
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
HXB
Product Code Name
Probe
Public Device Record Key
13be34e0-ec69-4a53-b1d7-b18eca43cd9d
Public Version Date
May 23, 2022
Public Version Number
5
DI Record Publish Date
February 02, 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 | 1328 |
2 | A medical device with a moderate to high risk that requires special controls. | 3995 |