Multi Cylinder Screw

GUDID 08809971099868

ARUM DENTISTRY Co., Ltd.

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 08809971099868
• NIH Device Record Key: fe875670-2927-4da2-a7c5-22add102f1bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Multi Cylinder Screw
• Version Model Number: MUCS1821
• Company DUNS: 557821945
• Company Name: ARUM DENTISTRY Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• 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	08809971099868 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K241703

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[08809971099868]

Moist Heat or Steam Sterilization

[08809971099868]

Moist Heat or Steam Sterilization

[08809971099868]

Moist Heat or Steam Sterilization

[08809971099868]

Moist Heat or Steam Sterilization

[08809971099868]

Moist Heat or Steam Sterilization

[08809971099868]

Moist Heat or Steam Sterilization

[08809971099868]

Moist Heat or Steam Sterilization

[08809971099868]

Moist Heat or Steam Sterilization

[08809971099868]

Moist Heat or Steam Sterilization

[08809971099868]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-03-20
• Device Publish Date: 2026-03-12

On-Brand Devices [Multi Cylinder Screw]

• 08809971099875: NMUCS1821
• 08809971099868: MUCS1821