Dri-Scope Aid - Cabinet - Pump Wall (P3R) - Series 1840 - Dri-Scope Aid-Cabinet; Pump Wall BL1; Series - TRICOR SYSTEMS, INC.

Duns Number:070164694

Device Description: Dri-Scope Aid-Cabinet; Pump Wall BL1; Series 1840; DSAC-PW3-TSI; TRICOR Label; Reburbished Dri-Scope Aid-Cabinet; Pump Wall BL1; Series 1840; DSAC-PW3-TSI; TRICOR Label; Reburbished;Dri-Scope Aid - Cabinet 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 indefinitely until the endoscope is removed from the system. This (TRICOR Systems Inc - built / TRICOR Systems Inc - labeled) wall-mounted pump version is one component of the Dri-Scope Aid – Cabinet system that contains an internal pump used to provide HEPA filtered air to other parts of the system. This pump component is used along with 2 (or 1) of the Dri-Scope Aid - Manifolds which together works as a drying system. This pump component has been refurbished to a condition of safety and effectiveness that is comparable to when new.

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More Product Details

Catalog Number

DCPW-BL1-TSI

Brand Name

Dri-Scope Aid - Cabinet - Pump Wall (P3R) - Series 1840

Version/Model Number

DCPW-BL1-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"

Yes

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

b051e071-a925-4d70-b21c-559263c7e3b7

Public Version Date

August 28, 2020

Public Version Number

1

DI Record Publish Date

August 20, 2020

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