Ceramir® Restore QuikCap

Basic Information

• Brand Name: Ceramir® Restore QuikCap
• Primary DI: 07350052430335
• Version / Model: 40039
• Catalog Number: 40039
• Company Name: Doxa Dental AB
• Labeler DUNS: 350486340
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 5
• Record Status: Published
• Publish Date: 2020-12-31
• Public Version: 2
• Public Version Date: 2023-04-19
• Public Version Status: Update
• Public Device Record Key: ad1ae1d5-3ba7-4dc7-9279-fab53eb79479

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
EMA	Cement, Dental	Dental	872.3275	2

GMDN Terms

Code	Name	Definition	Implantable	Status
16704	Glass ionomer dental cement	A non-sterile substance intended for professional use as a dental cement (e.g., luting agent, liner, base, pulp-capping material) and/or direct dental restorative material whereby the majority of the setting reaction is based on the hardening reaction between an aluminosilicate glass powder and an aqueous solution of a polyalkenoic acid. It typically includes some additional fillers, and may include setting substances that are in the minority (e.g., resin, metal). After application, this device cannot be reused.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Unit of Use	07350052430311	GS1
Primary	07350052430335	GS1

Customer Contacts

• Phone: 1.855.369-2872
• Email: [email protected]

Premarket Submissions

Submission Number	Supplement Number
K201937	000