Duns Number:025460908
Device Description: BIOPSY VALVE STRL OLYMP FUJI
Catalog Number
DYNDVALVEO
Brand Name
MEDLINE
Version/Model Number
DYNDVALVEO
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"
Yes
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
OCX
Product Code Name
endoscopic irrigation/suction system
Public Device Record Key
6f452ee0-29ae-49eb-bf7a-bdb4e929d6df
Public Version Date
March 19, 2021
Public Version Number
2
DI Record Publish Date
May 18, 2020
Package DI Number
40888277085665
Quantity per Package
100
Contains DI Package
10888277085664
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 38540 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 85094 |
| 3 | A medical device with high risk that requires premarket approval | 2 |
| U | Unclassified | 7 |