Dri-Scope Aid - [Gen 2] Cabinet - Manifold (M1) - Series 3316 - Dri-Scope Aid-Cabinet [Gen 2]; Manifold; Series - TRICOR SYSTEMS, INC.

Duns Number:070164694

Device Description: Dri-Scope Aid-Cabinet [Gen 2]; Manifold; Series 3316; DSC2-M1-3316-TSI; TRICOR Label;Dri-S Dri-Scope Aid-Cabinet [Gen 2]; Manifold; Series 3316; DSC2-M1-3316-TSI; TRICOR Label;Dri-Scope Aid - Cabinet Gen 2 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.

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More Product Details

Catalog Number

DC2M3316-TSI

Brand Name

Dri-Scope Aid - [Gen 2] Cabinet - Manifold (M1) - Series 3316

Version/Model Number

DC2M3316-TSI

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

MNL

Product Code Name

Accessories, Cleaning Brushes, For Endoscope

Device Record Status

Public Device Record Key

806d3dec-3d86-4957-8bbb-ef402c96bc25

Public Version Date

February 16, 2022

Public Version Number

1

DI Record Publish Date

February 08, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"TRICOR SYSTEMS, INC." Characteristics
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