Mixing pad

GUDID E22123031

VOCO GmbH

Dental material injection cannula, single-use

• Primary Device ID: E22123031
• NIH Device Record Key: a7862458-729a-4713-88d3-980910562eb6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mixing pad
• Version Model Number: 2303
• Company DUNS: 316699578
• Company Name: VOCO GmbH
• Device Count: 4
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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: 999-999-9999
• Email: xxx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E2212303 [Unit of Use]
HIBCC	E22123031 [Primary]

FDA Product Code

• EJB: Handle, Instrument, 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: 2019-08-21
• Device Publish Date: 2019-05-03

On-Brand Devices [Mixing pad]

• E22123031: 2303
• E22123021: 2302