Duns Number:103977526
Device Description: Extension for use with Universal Couchtop™ Long Extension
Catalog Number
MTIL6676
Brand Name
UCT XLE Standard Profile
Version/Model Number
MTIL6676
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
K180021
Product Code
IXQ
Product Code Name
Table, radiographic, stationary top
Public Device Record Key
33abbdf7-51aa-4677-973d-a09b06e6595a
Public Version Date
December 22, 2020
Public Version Number
2
DI Record Publish Date
June 21, 2019
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 | 31 |
2 | A medical device with a moderate to high risk that requires special controls. | 1027 |