MICROPRIME

GUDID 00840481135309

Black Flocked Tip, 22 gauge

Zest Anchors, LLC

Dental material injection cannula, single-use

• Primary Device ID: 00840481135309
• NIH Device Record Key: c8883db2-8959-4ce5-8f98-4a3324cfad43
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MICROPRIME
• Version Model Number: 90-00251
• Company DUNS: 078387192
• Company Name: Zest Anchors, LLC
• Device Count: 20
• 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: +1 877-918-4060
• Email: quality@zestdent.com
• Phone: +1 877-918-4060
• Email: quality@zestdent.com
• Phone: +1 877-918-4060
• Email: quality@zestdent.com
• Phone: +1 877-918-4060
• Email: quality@zestdent.com
• Phone: +1 877-918-4060
• Email: quality@zestdent.com
• Phone: +1 877-918-4060
• Email: quality@zestdent.com
• Phone: +1 877-918-4060
• Email: quality@zestdent.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840481135309 [Primary]
GS1	10840481135306 [Unit of Use]

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-03-18
• Device Publish Date: 2026-03-10

On-Brand Devices [MICROPRIME]

• 00840481135309: Black Flocked Tip, 22 gauge
• 00840481135293: MicroPrime G Desensitizer Gel, 4 - 1 mL syringes, 20 Tips
• 00840481135286: MicroPrime G Desensitizer Gel, 1 - 4 mL syringe, 20 Tips