Automix-Dispenser Type 50 1:1 999507

GUDID EDMG9995071

Automix-Dispenser Type 50 1:1. Suitable for Honigum Pro Mono, Honigum Pro Heavy, Honigum Pro Heavy Scan, Honigum Mono, Honigum Heavy, O-Bite, O-Bite Scan, Honigum Pro Light, Honigum Light. Content: 1 dispenser.

DMG Chemisch-Pharmazeutische Fabrik GmbH

Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual Dental material cartridge-plunging applicator, two-component, manual

• Primary Device ID: EDMG9995071
• NIH Device Record Key: 8289298a-ef5d-471a-ba69-35db511f87ec
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Automix-Dispenser Type 50 1:1
• Version Model Number: 999507
• Catalog Number: 999507
• Company DUNS: 320744915
• Company Name: DMG Chemisch-Pharmazeutische Fabrik GmbH
• 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: 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: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com
• Phone: 201-894-5505
• Email: ccosta@dmg-america.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EDMG9995071 [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: 2022-09-09
• Device Publish Date: 2022-09-01

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