Ultradent Cheek Retractor 4872

GUDID 00883205030719

Ultradent Cheek Retractor Large (Black)

ULTRADENT PRODUCTS, INC.

Dental cheek retractor, professional, single-use

• Primary Device ID: 00883205030719
• NIH Device Record Key: 9b05faf0-65c9-48f2-8a91-2588317fea24
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ultradent Cheek Retractor
• Version Model Number: 4872
• Catalog Number: 4872
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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

Customer Support Contacts

• Phone: +1(801)572-4200
• Email: customerservice@ultradent.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00883205030719 [Primary]

FDA Product Code

• EIG: RETRACTOR, ALL TYPES

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: 2019-07-29
• Device Publish Date: 2019-07-19

On-Brand Devices [Ultradent Cheek Retractor]

• 00883205030719: Ultradent Cheek Retractor Large (Black)
• 00883205030702: Ultradent Cheek Retractor Medium (Black)
• 00883205030696: Ultradent Cheek Retractor Medium (Clear)
• 00883205032492: Ultradent Cheek Retractor Medium (Clear)
• 00883205032485: Ultradent Cheek Retractor Medium (Clear)