Guide Drill

GUDID 08800039307802

InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)

Fixture/appliance dental drill bit, reusable

• Primary Device ID: 08800039307802
• NIH Device Record Key: bfdd1f00-f3ab-4d62-92c9-c6f29efcca5e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guide Drill
• Version Model Number: 1.6GD
• Company DUNS: 631169224
• Company Name: InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• 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	08800039307802 [Primary]

FDA Product Code

• DZA: Drill, Dental, Intraoral

Sterilization

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

[08800039307802]

Moist Heat or Steam Sterilization

[08800039307802]

Moist Heat or Steam Sterilization

[08800039307802]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-09-01
• Device Publish Date: 2022-04-11

On-Brand Devices [Guide Drill]

• 08800039307864: 2.8GD
• 08800039307802: 1.6GD