AccessGUDID - DEVICE: Dri-Scope Aid - Power Supply (w/6 ft cord) (00810053601006)

GUDID

Device Identifier (DI) Information

Brand Name: Dri-Scope Aid - Power Supply (w/6 ft cord)
Version or Model: 401789-146
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 401789-146
Company Name: TRICOR SYSTEMS, INC.

Primary DI Number: 00810053601006
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 070164694 *Terms of Use

Device Description: Dri-Scope Aid Jet-Stream; Power Supply; qty 1; Medical Grade. Consult TRICOR Systems Inc regarding Dri-Scope Aid Jet-Stream maintenance & service items to support your device & maintain compliance

Device Characteristics

What MRI safety information does the labeling contain?	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):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
65046	Endoscope dryer	An electrically-powered assembly of devices designed to dry the internal channel of an endoscope after washing, and to maintain dryness during storage, to prevent bacterial growth and endoscope deterioration. It consists of a user interface, a control unit, tubing/connectors for attaching to the endoscope, and may incorporate either an internal air pump or a connection for standard medical air supply; it may be designed for use on a bench or in a cabinet.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MNL	Accessories, Cleaning Brushes, For Endoscope

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: f19112b8-bc56-41c8-af59-e9f20bc3dc89
Public Version Date: April 02, 2025
Public Version Number: 1
DI Record Publish Date: March 25, 2025