ACT®

Basic Information

• Brand Name: ACT®
• Primary DI: 00844868000457
• Version / Model: ACTDE
• Company Name: BIOMET 3I, LLC
• Labeler DUNS: 186127825
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2015-10-06
• Public Version: 4
• Public Version Date: 2022-03-10
• Public Version Status: Update
• Public Device Record Key: a0e5d709-804a-4d7e-9827-4c0b7f8d0185

Device Description

ACT® DRILL EXTENSION

Device Characteristics

• Single Use: No
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: Yes
• Sterilization Methods: Moist Heat or Steam Sterilization

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
NDP	ACCESSORIES, IMPLANT, DENTAL, ENDOSSEOUS	Dental	872.3980	1

GMDN Terms

Code	Name	Definition	Implantable	Status
45320	Dental drill bit extension	A device intended to be attached to the shaft of a normal dental drill bit in order to lengthen it, providing greater accessibility and/or drilling capacity during a dental procedure. It is typically made of a high-grade metal [e.g., stainless steel, titanium (Ti)]. This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00844868000457	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]