Dynax® light D6103

GUDID E239D61031

No.

Dreve Dentamid GmbH

Silicone dental impression material

• Primary Device ID: E239D61031
• NIH Device Record Key: 92e2e6a4-f949-4a1b-85e8-ec151462f933
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dynax® light
• Version Model Number: D6103
• Catalog Number: D6103
• Company DUNS: 388000846
• Company Name: Dreve Dentamid GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: +49230388070
• Email: info@dreve.de

Operating and Storage Conditions

• Storage Environment Temperature: Between 18 Degrees Celsius and 28 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E239D61031 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K171562

FDA Product Code

• ELW: Material, Impression

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-01-24
• Device Publish Date: 2018-04-18

On-Brand Devices [Dynax® light]

• E239D61041: No.
• E239D61031: No.