DIO Remove Bar

GUDID 08800049202401

DIO Corporation

Dental prosthesis removal instrument

• Primary Device ID: 08800049202401
• NIH Device Record Key: e719dcd5-6b5d-4c7a-bba4-71232af69ea0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DIO Remove Bar
• Version Model Number: RB 34
• Company DUNS: 631085206
• Company Name: DIO Corporation
• Device Count: 1
• DM Exempt: true
• 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: 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	08800049202401 [Primary]

FDA Product Code

• DZN: Instruments, Dental Hand

Sterilization

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

[08800049202401]

Moist Heat or Steam Sterilization

[08800049202401]

Moist Heat or Steam Sterilization

[08800049202401]

Moist Heat or Steam Sterilization

[08800049202401]

Moist Heat or Steam Sterilization

[08800049202401]

Moist Heat or Steam Sterilization

[08800049202401]

Moist Heat or Steam Sterilization

[08800049202401]

Moist Heat or Steam Sterilization

[08800049202401]

Moist Heat or Steam Sterilization

[08800049202401]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-04-18
• Device Publish Date: 2022-12-08

On-Brand Devices [DIO Remove Bar]

• 08800049202401: RB 34
• 08800049202395: RB 32