Qu-resin pink 54001161

GUDID EBRE540011619

Qu-resin pink 1 Assortment

bredent GmbH & Co. KG

Dental composite resin

• Primary Device ID: EBRE540011619
• NIH Device Record Key: 77a8f95e-e1ea-4664-a0cd-061d7bf8323d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Qu-resin pink
• Version Model Number: 54001161
• Catalog Number: 54001161
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

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

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight
• Special Storage Condition, Specify: Between 0 and 0 *keep out of sunlight

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EBRE540011610 [Primary]
HIBCC	EBRE540011619 [Package]; Contains: EBRE540011610; Package: dummy [1 Units]; Discontinued: 2023-09-07; Not in Commercial Distribution

FDA Product Code

• EKO: Denture preformed (partially prefabricated denture)

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: 2023-09-15
• Device Publish Date: 2023-09-07

On-Brand Devices [Qu-resin pink]

• EBRE540011659: Qu-resin pink 50 ml
• EBRE540011619: Qu-resin pink 1 Assortment