Safesider HF 5104-G30

GUDID 00766054002833

SafeSiders HF Gutta Percha 30/04

ESSENTIAL DENTAL SYSTEMS, INC.

Root canal obturating point Root canal obturating point Root canal obturating point Root canal obturating point Root canal obturating point Root canal obturating point Root canal obturating point Root canal obturating point Root canal obturating point Root canal obturating point Root canal obturating point Root canal obturating point Root canal obturating point

• Primary Device ID: 00766054002833
• NIH Device Record Key: 9b07b0d0-9ce7-4c96-bd79-4f69a38a3b2b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Safesider HF
• Version Model Number: 5104-G30
• Catalog Number: 5104-G30
• Company DUNS: 101147171
• Company Name: ESSENTIAL DENTAL SYSTEMS, INC.
• 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: 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

Customer Support Contacts

• Phone: +1(201)487-9090
• Email: udi@edsdental.com
• Phone: +1(201)487-9090
• Email: udi@edsdental.com
• Phone: +1(201)487-9090
• Email: udi@edsdental.com
• Phone: +1(201)487-9090
• Email: udi@edsdental.com
• Phone: +1(201)487-9090
• Email: udi@edsdental.com
• Phone: +1(201)487-9090
• Email: udi@edsdental.com
• Phone: +1(201)487-9090
• Email: udi@edsdental.com
• Phone: +1(201)487-9090
• Email: udi@edsdental.com
• Phone: +1(201)487-9090
• Email: udi@edsdental.com
• Phone: +1(201)487-9090
• Email: udi@edsdental.com
• Phone: +1(201)487-9090
• Email: udi@edsdental.com
• Phone: +1(201)487-9090
• Email: udi@edsdental.com
• Phone: +1(201)487-9090
• Email: udi@edsdental.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00766054002833 [Primary]

FDA Product Code

• EKM: GUTTA-PERCHA

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: 2020-07-27
• Device Publish Date: 2020-07-17

On-Brand Devices [Safesider HF]

• 00766054002833: SafeSiders HF Gutta Percha 30/04
• 00766054002826: SafeSiders HF Gutta Percha 25/04
• 00766054002819: Safesider HF Glidepath Refill 25 mm
• 00766054002802: Safesider HF Shaper Refill 25 mm
• 00766054002796: Safesider HF Finisher Refill 25 mm
• 00766054002789: Safesider HF Finisher Refill 21 mm
• 00766054002772: Safesider HF Shaper Refill 21 mm
• 00766054002765: Safesider HF Glidepath Refill 21 mm
• 00766054002758: Safesider HF Intro Kit 25 mm
• 00766054002741: Safesider HF Intro Kit 21 mm