Duns Number:868205779
Device Description: The Quick Connect for Intuitive Surgical Ion Fully Articulating Catheter and Peripheral Vi The Quick Connect for Intuitive Surgical Ion Fully Articulating Catheter and Peripheral Vision Probe used with the C1220E Directed Flow Processing Container and Tray when used in the SYSTEM 1E and SYSTEM 1 endo Liquid Chemical Sterilant Processing Systems.
Catalog Number
QMC1771E
Brand Name
NA
Version/Model Number
Quick Connect
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)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K090036,K101409,K102462,K113520,K131078,K161683,K170956,K173256,K180342,K182827,K190104,K191343,K192929,K210737,K211607,K222615
Product Code
MED
Product Code Name
Sterilant, medical devices
Public Device Record Key
b8f3fa52-860d-4a19-8f0a-c55958a2409e
Public Version Date
October 25, 2022
Public Version Number
6
DI Record Publish Date
June 04, 2020
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 1528 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1557 |