Tap Drill

GUDID 08800070237021

Izenimplant Co., Ltd.

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

• Primary Device ID: 08800070237021
• NIH Device Record Key: 8223eff8-0525-4cf2-b9cf-c64ab4a19911
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tap Drill
• Version Model Number: TD4FF40
• Company DUNS: 694625347
• Company Name: Izenimplant Co., Ltd.
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800070237021 [Primary]

FDA Product Code

• DZA: Drill, Dental, Intraoral

Sterilization

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

[08800070237021]

Moist Heat or Steam Sterilization

[08800070237021]

Moist Heat or Steam Sterilization

[08800070237021]

Moist Heat or Steam Sterilization

[08800070237021]

Moist Heat or Steam Sterilization

[08800070237021]

Moist Heat or Steam Sterilization

[08800070237021]

Moist Heat or Steam Sterilization

[08800070237021]

Moist Heat or Steam Sterilization

[08800070237021]

Moist Heat or Steam Sterilization

[08800070237021]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-07-03
• Device Publish Date: 2025-06-25

On-Brand Devices [Tap Drill]

• 08800070237045: TD4FF50
• 08800070237038: TD4FF45
• 08800070237021: TD4FF40
• 08800070237014: TD4FF35