Dri-Scope Aid - Cabinet - Pump Wall (P3R) - Series 1840 - Mob Aspects DCPW-BL1-MOB

GUDID 00810053600573

Dri-Scope Aid-Cabinet; Pump Wall BL1; Series 1840; DSAC-PW3-MOB-R; TRICOR Label; Refurbished; 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. Note: this system has been programmed to accept external software commands and/or remote monitoring via Mobile Aspects proprietary hardware and software. 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 ID00810053600573
NIH Device Record Key5d73b2b5-eb35-40bf-8bec-1d729a10a671
Commercial Distribution StatusIn Commercial Distribution
Brand NameDri-Scope Aid - Cabinet - Pump Wall (P3R) - Series 1840 - Mob Aspects
Version Model NumberDCPW-BL1-MOB
Catalog NumberDCPW-BL1-MOB
Company DUNS070164694
Company NameTRICOR SYSTEMS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100810053600573 [Primary]

FDA Product Code

MNLAccessories, Cleaning Brushes, For Endoscope

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-03-10
Device Publish Date2023-03-02

Devices Manufactured by TRICOR SYSTEMS, INC.

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