Ease-In-Shields 5841

GUDID 00883205037497

Industrial/ R&D Edition Ease-In-Shields

ULTRADENT PRODUCTS, INC.

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• Primary Device ID: 00883205037497
• NIH Device Record Key: 1d28bd20-5978-44d5-83ad-cb0012cb5880
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ease-In-Shields
• Version Model Number: 5841
• Catalog Number: 5841
• Company DUNS: 013369913
• Company Name: ULTRADENT PRODUCTS, INC.
• 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: 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

Customer Support Contacts

• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com
• Phone: 801-572-4200
• Email: customerservice@ultradent.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00883205037497 [Primary]

FDA Product Code

• HOY: Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-11-03
• Device Publish Date: 2023-10-26

On-Brand Devices [Ease-In-Shields]

• 00883205037459: Dual Wave Ease-In-Shields
• 00883205037442: CO2 Ease-In-Shields
• 00883205037435: Universal Hard Tissue Ease-in-Shields
• 00883205037428: Universal Soft Tissue Ease-in-Shields
• 00883205037480: Aviation Ease-In-Shields
• 00883205037473: Curing Light Ease-In-Shields
• 00883205037466: Diode Soft Tissue Ease-In-Shields
• 00883205037541: NDYAG and ERYAG Ease-In-Shields
• 00883205037534: TriWave Ease-In-Shields
• 00883205037527: CO2 Ease-In-Shields
• 00883205037510: Pink Diode Soft Tissue Edition Ease-In-Shields
• 00883205037503: Multi-Wave Ease-In-Shields
• 00883205037497: Industrial/ R&D Edition Ease-In-Shields