Guide Fixture Driver Machine

GUDID 08809982753933

ARUM DENTISTRY Co., Ltd.

Surgical screwdriver, reusable

• Primary Device ID: 08809982753933
• NIH Device Record Key: 7b5ba918-9cf0-484e-ab83-0720bf76d3c8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guide Fixture Driver Machine
• Version Model Number: GFDM29M
• Company DUNS: 557821945
• Company Name: ARUM DENTISTRY 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: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809982753933 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[08809982753933]

Moist Heat or Steam Sterilization

[08809982753933]

Moist Heat or Steam Sterilization

[08809982753933]

Moist Heat or Steam Sterilization

[08809982753933]

Moist Heat or Steam Sterilization

[08809982753933]

Moist Heat or Steam Sterilization

[08809982753933]

Moist Heat or Steam Sterilization

[08809982753933]

Moist Heat or Steam Sterilization

[08809982753933]

Moist Heat or Steam Sterilization

[08809982753933]

Moist Heat or Steam Sterilization

[08809982753933]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-04-01
• Device Publish Date: 2026-03-24

On-Brand Devices [Guide Fixture Driver Machine]

• 08809982753940: GFDM30R
• 08809982753933: GFDM29M
• 08800341411785: MGFDM29
• 08800265646560: GFDM31M
• 08800265646492: GFDM31R