Skini Syringe 1680

GUDID 00883205019578

Skini Syringes 20pk

ULTRADENT PRODUCTS, INC.

General-purpose syringe, single-use

• Primary Device ID: 00883205019578
• NIH Device Record Key: d035d004-3682-4dd6-8394-d3573bab5d45
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Skini Syringe
• Version Model Number: 1680
• Catalog Number: 1680
• 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	00883205019578 [Primary]

FDA Product Code

• EIC: SYRINGE, PERIODONTIC, ENDODONTIC, IRRIGATING

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: 2018-09-12
• Device Publish Date: 2018-06-13

On-Brand Devices [Skini Syringe]

• 00883205019578: Skini Syringes 20pk
• 00883205004871: Skini Syringes 50pk
• 00883205004598: Skini Syringe Clear 20pk