Single Patient ACT® Twist Drill, 2mmD x 10mmL

GUDID 00844868051831

Single Patient ACT® Twist Drill, 2mmD x 10mmL

BIOMET 3I, LLC

Fixture/appliance dental drill bit, single-use

• Primary Device ID: 00844868051831
• NIH Device Record Key: c9980261-4d94-4956-a3c3-499c03da8b52
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Single Patient ACT® Twist Drill, 2mmD x 10mmL
• Version Model Number: SPACT2010
• Company DUNS: 186127825
• Company Name: BIOMET 3I, LLC
• 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: true
• 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(800)342-5454
• Email: dentalCS@zimvie.com
• Phone: +1(800)342-5454
• Email: dentalCS@zimvie.com
• Phone: +1(800)342-5454
• Email: dentalCS@zimvie.com
• Phone: +1(800)342-5454
• Email: dentalCS@zimvie.com
• Phone: +1(800)342-5454
• Email: dentalCS@zimvie.com
• Phone: +1(800)342-5454
• Email: dentalCS@zimvie.com
• Phone: +1(800)342-5454
• Email: dentalCS@zimvie.com
• Phone: +1(800)342-5454
• Email: dentalCS@zimvie.com
• Phone: +1(800)342-5454
• Email: dentalCS@zimvie.com
• Phone: +1(800)342-5454
• Email: dentalCS@zimvie.com
• Phone: +1(800)342-5454
• Email: dentalCS@zimvie.com
• Phone: +1(800)342-5454
• Email: dentalCS@zimvie.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00844868051831 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

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: 2025-12-26
• Device Publish Date: 2025-12-18

Devices Manufactured by BIOMET 3I, LLC

• 00844868051824 - Single Patient ACT® Twist Drill: 2025-12-26 Single Patient ACT® Twist Drill, 2mmD x 15mmL
• 00844868051831 - Single Patient ACT® Twist Drill, 2mmD x 10mmL: 2025-12-26Single Patient ACT® Twist Drill, 2mmD x 10mmL
• 00844868051831 - Single Patient ACT® Twist Drill, 2mmD x 10mmL: 2025-12-26 Single Patient ACT® Twist Drill, 2mmD x 10mmL
• 00844868051848 - Single Patient ACT® Twist Drill: 2025-12-26 Single Patient ACT® Twist Drill, 2mmD x 20mmL
• 00844868051855 - Single Patient ACT® Twist Drill: 2025-12-26 Single Patient ACT® Twist Drill, 2mmD x 6mmL
• 00844868051862 - Single Patient ACT® Twist Drill: 2025-12-26 Single Patient ACT® Twist Drill, 2.75mmD x 10mmL
• 00844868051879 - Single Patient ACT® Twist Drill: 2025-12-26 Single Patient ACT® Twist Drill, 2.75mmD x 15mmL
• 00844868051886 - Single Patient ACT® Twist Drill: 2025-12-26 Single Patient ACT® Twist Drill, 2.75mmD x 20mmL
• 00844868051893 - Single Patient ACT® Twist Drill: 2025-12-26 Single Patient ACT® Twist Drill, 3mmD x 10mmL