Guide Pin 260-101-183

GUDID 00813110024244

3.0mm Standard Guide Pin

BICON, LLC

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 00813110024244
• NIH Device Record Key: ae6f66b9-0a5d-41f6-928f-b185e8c6ecfa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guide Pin
• Version Model Number: 260-101-183
• Catalog Number: 260-101-183
• Company DUNS: 945015758
• Company Name: BICON, LLC
• Device Count: 4
• 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: false
• 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: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813110024244 [Primary]
GS1	10813110024241 [Unit of Use]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[00813110024244]

Moist Heat or Steam Sterilization

[00813110024244]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-03-25
• Device Publish Date: 2016-05-06

On-Brand Devices [Guide Pin]

• 00813110024251: 2.5mm Standard Guide Pin
• 00813110024244: 3.0mm Standard Guide Pin
• 00813110024237: 2.0mm Standard Guide Pin
• 10813110024234: 2.5mm Guide Pin - Tall Post (4)