Black Mini Tip 514

GUDID 00883205021786

Black Mini Tips 100pk

ULTRADENT PRODUCTS, INC.

Surgical/emergency suction cannula, non-illuminating, single-use

• Primary Device ID: 00883205021786
• NIH Device Record Key: 707e8438-ef1b-4159-90a2-e84119d04223
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Black Mini Tip
• Version Model Number: 514
• Catalog Number: 514
• 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	00883205021786 [Primary]

FDA Product Code

• EID: SYRINGE, RESTORATIVE AND IMPRESSION MATERIAL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-02-21
• Device Publish Date: 2018-04-28

On-Brand Devices [Black Mini Tip]

• 00883205022363: Black Mini Tips 500pk
• 00883205021786: Black Mini Tips 100pk
• 00883205021663: Black Mini Tips 20pk