Dri-Scope Aid - [Gen 2] Cabinet - Pump Ceiling (P3R) - Series 1840 DCPC-BL1-TSI2

GUDID 00810053600597

Dri-Scope Aid-Cabinet [Gen 2]; Pump Ceiling BL1; Series 1840; DSC2-PC3-TSI-R; TRICOR Label; Refurbished; 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 indefinitely until the endoscope is removed from the system. This (TRICOR Systems Inc - built / TRICOR Systems Inc - labeled) ceiling-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 component has been refurbished to a condition of safety and effectiveness that is comparable to when new.

TRICOR SYSTEMS, INC.

Endoscope dryer

• Primary Device ID: 00810053600597
• NIH Device Record Key: dd6b73e5-bcee-4dc8-8524-3e35b39f4ea8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dri-Scope Aid - [Gen 2] Cabinet - Pump Ceiling (P3R) - Series 1840
• Version Model Number: DCPC-BL1-TSI2
• Catalog Number: DCPC-BL1-TSI2
• Company DUNS: 070164694
• Company Name: TRICOR SYSTEMS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810053600597 [Primary]

FDA Product Code

• MNL: Accessories, Cleaning Brushes, For Endoscope

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-03-10
• Device Publish Date: 2023-03-02

Devices Manufactured by TRICOR SYSTEMS, INC.

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