AccessGUDID - DEVICE: Reveal (00724995184735)

GUDID

Device Identifier (DI) Information

Brand Name: Reveal
Version or Model: 00711770
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 00711770
Company Name: US Endoscopy

Primary DI Number: 00724995184735
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 627879687 *Terms of Use
Previous DI: 00816765012642

Device Description: The Reveal distal attachment cap is attached to the distal end of the endoscope to facilitate endoscopic therapy and is intended for gastrointestinal mucosal resection (endoscopic mucosal resection) and keeping the suitable depth of endoscope's view field.

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":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	Yes
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?
58841	Endoscope tissue removal cap, single-use	A plastic tube designed to be placed onto the distal end of an endoscope (e.g., oesophagoscope) to facilitate the removal of coagulated blood/tissue from the path of the endoscope during endoscopic surgery. It is designed to fit tightly without fixing, having an oblique leading edge that extends beyond the end of the endoscope to provide atraumatic penetration and tissue removal functionality (e.g., scooping, grasping). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OCX	endoscopic irrigation/suction system

FDA Premarket Submission

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

Device Exempt from Premarket Submission: No CLOSE

Sterilization

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

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Keep Dry

Clinically Relevant Size

[?]

Size Type Text
Outer Diameter: 11 Millimeter

Device Record Status

Public Device Record Key: b695454e-64ef-41c8-9116-0268e295b41c
Public Version Date: April 07, 2021
Public Version Number: 3
DI Record Publish Date: April 01, 2020