Black Micro FX Tip 1357

GUDID 00883205022141

Black Micro FX Tips 100pk

ULTRADENT PRODUCTS, INC.

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

• Primary Device ID: 00883205022141
• NIH Device Record Key: a7c18823-2988-4c9a-a6fa-3944df91693e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Black Micro FX Tip
• Version Model Number: 1357
• Catalog Number: 1357
• 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	00883205022141 [Primary]

FDA Product Code

• EIY: INSTRUMENT, FILLING, PLASTIC, DENTAL

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 Micro FX Tip]

• 00883205022370: Black Micro FX Tips 500pk
• 00883205022141: Black Micro FX Tips 100pk