Duns Number:713565195
Device Description: This product is intended to prevent backflow of body fluid etc, from the forceps port of e This product is intended to prevent backflow of body fluid etc, from the forceps port of endoscope and to enable to insert treatment devices into the body cavity by attaching the forceps port of endoscope.
Catalog Number
-
Brand Name
FUJIFILM
Version/Model Number
FV-001
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
Yes
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
FFY
Product Code Name
Adaptor, bulbs, miscellaneous, for endoscope
Public Device Record Key
2f2673ea-788b-4fa6-8d3a-ba9345c3fea0
Public Version Date
October 17, 2022
Public Version Number
1
DI Record Publish Date
October 07, 2022
Package DI Number
24547410391224
Quantity per Package
1
Contains DI Package
04547410391220
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
| 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 |