N/A 18060

GUDID D6901806020

Pediatric Class I & II Preparation Kit

Ss White Burs, Inc.

Carbide dental bur, single-use

• Primary Device ID: D6901806020
• NIH Device Record Key: 7dff40e5-8f2e-46a7-93dc-813496717777
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: N/A
• Version Model Number: N/A
• Catalog Number: 18060
• Company DUNS: 151760014
• Company Name: Ss White Burs, 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(732)905-1100
• Email: SSW-ALL-CustomerService@hu-friedy.com
• Phone: +1(732)905-1100
• Email: SSW-ALL-CustomerService@hu-friedy.com
• Phone: +1(732)905-1100
• Email: SSW-ALL-CustomerService@hu-friedy.com
• Phone: +1(732)905-1100
• Email: SSW-ALL-CustomerService@hu-friedy.com
• Phone: +1(732)905-1100
• Email: SSW-ALL-CustomerService@hu-friedy.com
• Phone: +1(732)905-1100
• Email: SSW-ALL-CustomerService@hu-friedy.com
• Phone: +1(732)905-1100
• Email: SSW-ALL-CustomerService@hu-friedy.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D6901806020 [Primary]

FDA Product Code

• EJL: BUR, DENTAL

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-01-26
• Device Publish Date: 2026-01-16

On-Brand Devices [N/A]

• D6901806020: Pediatric Class I & II Preparation Kit
• D6901805928: Calla Lilly Fissurotomy Class I & II Preparation Kit
• D6901805827: Calla Lilly Fissurotomy Class I Preparation Introductory Kit