URIS Scan Post Kit

GUDID 08800076474925

Truabutment Korea Co.,Ltd

Dental implant kit

• Primary Device ID: 08800076474925
• NIH Device Record Key: 509f1d9a-5d58-484a-84c5-85b4f4928ff9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: URIS Scan Post Kit
• Version Model Number: UOR-BETA
• Company DUNS: 694514760
• Company Name: Truabutment Korea 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: 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	08800076474925 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[08800076474925]

Moist Heat or Steam Sterilization

[08800076474925]

Moist Heat or Steam Sterilization

[08800076474925]

Moist Heat or Steam Sterilization

[08800076474925]

Moist Heat or Steam Sterilization

[08800076474925]

Moist Heat or Steam Sterilization

[08800076474925]

Moist Heat or Steam Sterilization

[08800076474925]

Moist Heat or Steam Sterilization

[08800076474925]

Moist Heat or Steam Sterilization

[08800076474925]

Moist Heat or Steam Sterilization

[08800076474925]

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 [URIS Scan Post Kit ]

• 08800076474925: UOR-BETA
• 08800076474918: UOR-ALPHA
• 08800076474901: UON-BETA
• 08800076474895: UON-ALPHA