Duns Number:068199363
Device Description: Pentax Endo Smartcap
Catalog Number
-
Brand Name
PENTAX ENDO SMARTCAP
Version/Model Number
100150CO2P
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 03, 2022
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
FAJ
Product Code Name
Cystoscope And Accessories, Flexible/Rigid
Public Device Record Key
8d8d0343-7ed7-4b26-99ba-f7da46d49ed9
Public Version Date
June 10, 2022
Public Version Number
6
DI Record Publish Date
October 10, 2018
Package DI Number
20677964060339
Quantity per Package
50
Contains DI Package
00677964060335
Package Discontinue Date
May 03, 2022
Package Status
Not 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 |