Duns Number:070164694
Device Description: DSA-Cabinet; Manifold; Series 3316; DSAC-M2-3316-TSI-R; TRICOR Label; Refurbished;Dri-Scop DSA-Cabinet; Manifold; Series 3316; DSAC-M2-3316-TSI-R; TRICOR Label; Refurbished;Dri-Scope Aid - Cabinet refurbished system is intended to aid in drying and venting internal channels of cleaned and disinfected endoscopes. The system is designed to cost-effectively convert existing passive cabinets (or closets) to active drying cabinets (or closets). The system can process as many as 16 endoscopes that are waiting in the queue. It provides pressure sensitive continuous flow of clean HEPA filtered air. Simply attach the endoscope, press the button to place the endoscope in the processing queue and the system will take care of the rest. After the drying cycle is complete, the system will periodically cycle dry air through the endoscope internal channels on a timed basis around the clock. This (TRICOR Systems Inc - built / TRICOR Systems Inc - labeled) 33” wide / 16 port manifold is one component of the Dri-Scope Aid – Cabinet system that receives the HEPA filtered air from the system pump and distributes it to the endoscope(s) for the purpose of drying and venting.
Catalog Number
DCM3316-TSI
Brand Name
Dri-Scope Aid - Cabinet - Manifold (M2R) - Series 3316 - Refurbished
Version/Model Number
DCM3316-TSI Refurbished
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)
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Device labeled as "Not made with natural rubber latex"
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For Single-Use
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Prescription Use (Rx)
-
Over the Counter (OTC)
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Kit
-
Combination Product
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Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
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FDA Premarket Submission
-
Product Code
MNL
Product Code Name
Accessories, Cleaning Brushes, For Endoscope
Public Device Record Key
655df915-b46c-46e3-b2a6-cd98249d1628
Public Version Date
July 05, 2022
Public Version Number
1
DI Record Publish Date
June 27, 2022
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 | 48 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1 |