EndoRings

GUDID 07290016767025

The EndoRings is intended to be attached to the distal end of the endoscope to facilitate endoscopic therapy, to be used for the following: Keeping th

ENDOAID LTD

Colonic endoscopy cuff

• Primary Device ID: 07290016767025
• NIH Device Record Key: 8668b791-4067-44a4-af0e-b5d9038c72b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EndoRings
• Version Model Number: E102
• Company DUNS: 600318101
• Company Name: ENDOAID LTD
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Height: 24 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290016767025 [Primary]
GS1	17290016767022 [Package]; Package: White carton box [15 Units]; In Commercial Distribution
GS1	27290016767029 [Package]; Contains: 17290016767022; Package: Master carton box [90 Units]; In Commercial Distribution

FDA Product Code

• FED: Endoscopic Access Overtube, Gastroenterology-Urology

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-27

On-Brand Devices [EndoRings]

• 07290016767032: The EndoRings is intended to be attached to the distal end of the endoscope to facilitate endosc
• 07290016767025: The EndoRings is intended to be attached to the distal end of the endoscope to facilitate endosc