Duns Number:314546664
Device Description: Being able to reduce attenuation in this scenario results in lower skin dose to the patien Being able to reduce attenuation in this scenario results in lower skin dose to the patient. The Connexion™ Central Opening Module provides a central opening where attenuation and dose build-up are minimized, allowing you to reduce skin doses.
Catalog Number
P10105-211
Brand Name
Connexion
Version/Model Number
P10105-211
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
IXQ
Product Code Name
Table, Radiographic, Stationary Top
Public Device Record Key
c1f9bacf-dddb-4c50-8187-b457be8e4eaa
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
August 23, 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 |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 175 |