Duns Number:713565195
Device Description: This product is intended to attach a balloon to a FUJIFILM endoscope in medical facilities This product is intended to attach a balloon to a FUJIFILM endoscope in medical facilities.
Catalog Number
-
Brand Name
FUJIFILM
Version/Model Number
BA-03
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
-
Product Code
FFY
Product Code Name
Adaptor, Bulbs, Miscellaneous, For Endoscope
Public Device Record Key
a625bdf9-48d4-4fac-80f6-0fd7f0d68a0f
Public Version Date
October 06, 2022
Public Version Number
1
DI Record Publish Date
September 28, 2022
Package DI Number
24547410432583
Quantity per Package
1
Contains DI Package
04547410432589
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 |