Duns Number:713565195
Device Description: This product is intended to clean the instrument/suction channel and accessories during pr This product is intended to clean the instrument/suction channel and accessories during pre-cleaning of a FUJIFILM endoscope.
Catalog Number
-
Brand Name
FUJIFILM
Version/Model Number
WB3212FW2
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"
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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
EOQ
Product Code Name
BRONCHOSCOPE (FLEXIBLE OR RIGID)
Public Device Record Key
e4c1fb33-0b6f-473c-8b90-b39a11d33205
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
October 18, 2016
Package DI Number
34547410079037
Quantity per Package
1
Contains DI Package
04547410079036
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Bag
| 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 |