NB Regular Kit

GUDID 08800055791210

ARUM DENTISTRY Co., Ltd.

Dental/maxillofacial surgical procedure kit, non-medicated, reusable

• Primary Device ID: 08800055791210
• NIH Device Record Key: b8fd8683-7dbb-4782-8245-cb627982f77f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NB Regular Kit
• Version Model Number: REK-SET
• 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	08800055791210 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[08800055791210]

Moist Heat or Steam Sterilization

[08800055791210]

Moist Heat or Steam Sterilization

[08800055791210]

Moist Heat or Steam Sterilization

[08800055791210]

Moist Heat or Steam Sterilization

[08800055791210]

Moist Heat or Steam Sterilization

[08800055791210]

Moist Heat or Steam Sterilization

[08800055791210]

Moist Heat or Steam Sterilization

[08800055791210]

Moist Heat or Steam Sterilization

[08800055791210]

Moist Heat or Steam Sterilization

[08800055791210]

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 [NB Regular Kit ]

• 08809982750802: REK2-SET
• 08800341412454: REK2C-SET
• 08800055791210: REK-SET