Duns Number:083211284
Device Description: C.A.P. HD DUODENOSCOPE (US NEW)
Catalog Number
-
Brand Name
VIDEO DUODENOSCOPE
Version/Model Number
ED34-I10T-US
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
K163614
Product Code
FDT
Product Code Name
Duodenoscope And Accessories, Flexible/Rigid
Public Device Record Key
dec845dd-2ef2-4eaf-889b-9835bc0422e4
Public Version Date
January 23, 2019
Public Version Number
3
DI Record Publish Date
March 12, 2018
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 | 247 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 425 |