DTK adhesive refill pack 54001195

GUDID EBRE540011959

DTK adhesive refill pack in a double mixing cartridge 1 x 8 g

bredent GmbH & Co. KG

Dental repair kit, ceramic

• Primary Device ID: EBRE540011959
• NIH Device Record Key: e446629b-181c-40d3-a98d-9691f8c11f30
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DTK adhesive refill pack
• Version Model Number: 54001195
• Catalog Number: 54001195
• Company DUNS: 341086190
• Company Name: bredent 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: 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +4907309872451
• Email: info@bredent.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EBRE540011950 [Primary]
HIBCC	EBRE540011959 [Package]; Contains: EBRE540011950; Package: dummy [1 Units]; Discontinued: 2016-09-22; Not in Commercial Distribution

FDA Product Code

• KOL: ADHESIVE, DENTURE, CARBOXYMETHYLCELLULOSE SODIUM (32%) AND ETHYLENE-OXIDE HOMOPOLYMER

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: 2018-03-29
• Device Publish Date: 2016-09-22

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