GUIDE PIN CONNECTOR

GUDID 08800020852496

SNUCONE Co.,LTD.

Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable

• Primary Device ID: 08800020852496
• NIH Device Record Key: e5eca9ca-83a4-46ca-a44c-cb06a5b5f043
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GUIDE PIN CONNECTOR
• Version Model Number: ABPC
• Company DUNS: 688806132
• Company Name: SNUCONE Co.,LTD.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• 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: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com
• Phone: 9999999999
• Email: snucone@naver.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800020852496 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

[08800020852496]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-03-01
• Device Publish Date: 2023-02-21

Devices Manufactured by SNUCONE Co.,LTD.

• 08800020818898 - DRILL EXTENSION: 2023-03-01
• 08800020818911 - LINDEMANN DRILL: 2023-03-01
• 08800020818928 - COUNTER SINK: 2023-03-01
• 08800020818935 - COUNTER SINK: 2023-03-01
• 08800020818942 - COUNTER SINK: 2023-03-01
• 08800020818959 - COUNTER SINK: 2023-03-01
• 08800020818966 - COUNTER SINK: 2023-03-01
• 08800020818973 - COUNTER SINK: 2023-03-01