EdgeFlow™ EE23GNRIN

GUDID 00818365028290

EdgeFlow E23G-NR Injection needle

US ENDODONTICS, LLC

Endodontic obturation material distribution endpiece, single-use

• Primary Device ID: 00818365028290
• NIH Device Record Key: 0f065824-7bda-4f97-8106-4f726e8e0520
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EdgeFlow™
• Version Model Number: EE23GNRIN
• Catalog Number: EE23GNRIN
• Company DUNS: 061317427
• Company Name: US ENDODONTICS, LLC
• Device Count: 1
• DM Exempt: true
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com
• Phone: +1(423)283-0047
• Email: Bobby.bennett@us-endo.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00818365028290 [Primary]

FDA Product Code

• EKR: PLUGGER, ROOT CANAL, ENDODONTIC

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: 2023-07-03
• Device Publish Date: 2023-06-25

On-Brand Devices [EdgeFlow™]

• 00818365028320: EdgeFlow E25G-NR Injection needle
• 00818365028313: EdgeFlow E25G-M Injection needle
• 00818365028306: EdgeFlow E25G-L Injection needle
• 00818365028290: EdgeFlow E23G-NR Injection needle
• 00818365028283: EdgeFlow E23G-M Injection needle
• 00818365028276: EdgeFlow E23G-L Injection needle
• 00818365028269: EdgeFlow E20G-S Injection needle
• 00818365028252: EdgeFlow E20G-NR Injection needle
• 00818365028245: EdgeFlow E20G-M Injection needle
• 00818365028238: EdgeFlow E20G-L Injection needle
• 00818365028115: EdgeFlow FiE-HS004 Heat Insulation Hood (3 Pack)
• 00818365028108: EdgeFlow FiE-HS003 Wrench
• 00818365028092: EdgeFlow FiE-HS002 Battery
• 00818365028085: EdgeFlow FiE-HS001 Charging Stand
• 00818365028078: EdgeFlow Fi-E (Pen-Type Obturator)