Duns Number:068199363
Catalog Number
-
Brand Name
ENDOGATOR Kit
Version/Model Number
100622B
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
K102855,K102855
Product Code
OCX
Product Code Name
Endoscopic Irrigation/Suction System
Public Device Record Key
7cc7832c-4e51-4f5f-b6c0-2fa88b9ea4e1
Public Version Date
April 27, 2022
Public Version Number
6
DI Record Publish Date
August 16, 2018
Package DI Number
20677964067376
Quantity per Package
20
Contains DI Package
00677964067372
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 | 2999 |
2 | A medical device with a moderate to high risk that requires special controls. | 362 |