Duns Number:005036025
Catalog Number
DPD6-G2Q
Brand Name
Midmark
Version/Model Number
DPD6-G2Q
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
K043092
Product Code
EHD
Product Code Name
Unit, x-ray, extraoral with timer
Public Device Record Key
a9f3fab9-5140-469f-8b88-760db21ea311
Public Version Date
January 25, 2021
Public Version Number
1
DI Record Publish Date
January 15, 2021
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 | 838 |
2 | A medical device with a moderate to high risk that requires special controls. | 544 |