Application cannulae

GUDID E22121311

Application cannulae type 47

VOCO GmbH

Dental material injection cannula, single-use

• Primary Device ID: E22121311
• NIH Device Record Key: 8f4e91d3-134e-443c-948b-a41e6972fbd8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Application cannulae
• Version Model Number: 2131
• Company DUNS: 316699578
• Company Name: VOCO GmbH
• Device Count: 30
• 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	E2212131 [Unit of Use]
HIBCC	E22121311 [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 [Application cannulae]

• E22123101: Application cannulae type 42
• E22121481: Application cannulae type 46
• E22121471: Application cannulae type 45
• E22121461: Application cannulae type 41
• E22121441: Application cannulae type 44
• E22121321: Application cannulae type 48
• E22121311: Application cannulae type 47