Honigum Pro 989767

GUDID EDMG9897671

VPS-based impression material. Heavy-bodied and light-bodied consistency. Impression made your way. Content: 2 cartridges Honigum Pro-Heavy @ 50 ml paste, 1 cartridge Honigum Pro-Light @ 50 ml paste, accessories.

DMG Chemisch-Pharmazeutische Fabrik GmbH

Silicone dental impression material

• Primary Device ID: EDMG9897671
• NIH Device Record Key: f493685f-0554-43d4-9e17-82d49c6f43c0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Honigum Pro
• Version Model Number: 989767
• Catalog Number: 989767
• Company DUNS: 320744915
• Company Name: DMG Chemisch-Pharmazeutische Fabrik 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• 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: 201-894-5505
• Email: eanagnostos@dmg-america.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 59 Degrees Fahrenheit and 77 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EDMG9897671 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K000878

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: 2018-07-06
• Device Publish Date: 2016-09-22

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