DIO Guide Sinus Approach Stopper

Basic Information

• Brand Name: DIO Guide Sinus Approach Stopper
• Primary DI: 08800049307465
• Version / Model: GST 10YE
• Company Name: DIO Corporation
• Labeler DUNS: 631085206
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2022-12-08
• Public Version: 1
• Public Version Date: 2022-12-16
• Public Version Status: New
• Public Device Record Key: 6ac6d00e-9d60-440a-ae45-e3295d4852c9

Device Characteristics

• Single Use: No
• Prescription Use (Rx): No
• 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: Yes
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: Yes
• 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
DZN	Instruments, Dental Hand	Dental	872.4565	1

GMDN Terms

Code	Name	Definition	Implantable	Status
65191	Dental instrument depth limiter	A small device in the form of a ring or cylinder intended to be placed on a surgically-invasive dental instrument or power tool endpiece (e.g., file/rasp, drill bit, reamer) to limit the depth of insertion typically into the tooth or bone; it is typically made of polymer materials (e.g., silicone). This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	08800049307465	GS1