Dynamic Mixers 17900

GUDID E217179001

Dynamic mixers, blue

Kettenbach GmbH & Co. KG

Dental impression material syringe, single-use

• Primary Device ID: E217179001
• NIH Device Record Key: 97db0767-5baf-47b3-9b6f-f471f5b369bc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dynamic Mixers
• Version Model Number: 17900
• Catalog Number: 17900
• Company DUNS: 316803246
• Company Name: Kettenbach GmbH & Co. KG
• 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: 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: +4927747050
• Email: info@kettenbach.de

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E217179001 [Primary]

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: 2018-12-28
• Device Publish Date: 2018-11-27

On-Brand Devices [Dynamic Mixers]

• E217179001: Dynamic mixers, blue
• E217179021: Dynamic mixers, 45 pieces