Screw Hex Remover Tool Guide

GUDID 08800341412386

ARUM DENTISTRY Co., Ltd.

Dental prosthesis removal instrument

• Primary Device ID: 08800341412386
• NIH Device Record Key: 7d2141f3-c0f1-4f8a-b2a6-00f76f71dea2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Screw Hex Remover Tool Guide
• Version Model Number: SRTG16
• 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	08800341412386 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[08800341412386]

Moist Heat or Steam Sterilization

[08800341412386]

Moist Heat or Steam Sterilization

[08800341412386]

Moist Heat or Steam Sterilization

[08800341412386]

Moist Heat or Steam Sterilization

[08800341412386]

Moist Heat or Steam Sterilization

[08800341412386]

Moist Heat or Steam Sterilization

[08800341412386]

Moist Heat or Steam Sterilization

[08800341412386]

Moist Heat or Steam Sterilization

[08800341412386]

Moist Heat or Steam Sterilization

[08800341412386]

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 [Screw Hex Remover Tool Guide]

• 08800341412393: SRTG20
• 08800341412386: SRTG16