JOTA

GUDID EJOT310105411297023

Jota AG

Steel dental bur, reusable

• Primary Device ID: EJOT310105411297023
• NIH Device Record Key: 47ffff48-0121-4b74-831e-6e356f0d2d78
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JOTA
• Version Model Number: 168.HPL.023
• Company DUNS: 480670983
• Company Name: Jota AG
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EJOT310105411297023 [Primary]

FDA Product Code

• GFF: Bur, Surgical, General & Plastic Surgery

Sterilization

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

[EJOT310105411297023]

Moist Heat or Steam Sterilization

[EJOT310105411297023]

Moist Heat or Steam Sterilization

[EJOT310105411297023]

Moist Heat or Steam Sterilization

[EJOT310105411297023]

Moist Heat or Steam Sterilization

[EJOT310105411297023]

Moist Heat or Steam Sterilization

[EJOT310105411297023]

Moist Heat or Steam Sterilization

[EJOT310105411297023]

Moist Heat or Steam Sterilization

[EJOT310105411297023]

Moist Heat or Steam Sterilization

[EJOT310105411297023]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-07-03
• Device Publish Date: 2025-06-25

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