NaviTip 31G Sideport 5122

GUDID 00883205022837

NaviTip 31g 21mm Sideport 50PK (Yellow)

ULTRADENT PRODUCTS, INC.

Syringe tip cap

• Primary Device ID: 00883205022837
• NIH Device Record Key: c4ff04e9-59aa-49a2-a4d8-011b65dc0988
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NaviTip 31G Sideport
• Version Model Number: 5122
• Catalog Number: 5122
• 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	00883205022837 [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: 2018-03-29
• Device Publish Date: 2017-07-26

On-Brand Devices [NaviTip 31G Sideport]

• 00883205022851: NaviTip 31g 27mm Sideport 50PK (Green)
• 00883205022844: NaviTip 31g 27mm Sideport 20PK (Green)
• 00883205022837: NaviTip 31g 21mm Sideport 50PK (Yellow)
• 00883205022820: NaviTip 31g 21mm Sideport 20PK (Yellow)