Duns Number:713565195
Device Description: This product is used for forward water conveyance to wash digestive tract in diagnosis wit This product is used for forward water conveyance to wash digestive tract in diagnosis with a water pump and our specified endoscope. This product is the tube for forward water conveyance to wash digestive tract in diagnosis, which connects between Water Jet inlet of Endoscope and a water pump.
Catalog Number
-
Brand Name
FUJIFILM
Version/Model Number
JA-500
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FDF
Product Code Name
Colonoscope and accessories, flexible/rigid
Public Device Record Key
28e3dd35-4cf8-4b7a-acff-4efc010f20f3
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
October 18, 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 |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 43 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 324 |
| 3 | A medical device with high risk that requires premarket approval | 1 |