MEDENTiKA

Basic Information

• Brand Name: MEDENTiKA
• Primary DI: EMKA02821ET9
• Version / Model: 0-28-21-ET
• Catalog Number: 0-28-21-ET
• Company Name: MEDENTiKA GmbH
• Labeler DUNS: 537555497
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2019-06-11
• Public Version: 1
• Public Version Date: 2019-06-19
• Public Version Status: New
• Public Device Record Key: 4a2eedd5-2730-4ae7-98a0-1b71674c795c

Device Description

MedentiBASE Labimplant

Device Characteristics

• Single Use: No
• 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: MR Conditional
• Direct Marking Exempt: Yes
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
NHA	ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS	Dental	872.3630	2

GMDN Terms

Code	Name	Definition	Implantable	Status
61642	Dental implant analog	A device intended to be used as a copy of a dental implant, for a dental laboratory working model, to duplicate the location and restorative platform orientation of the final dental implant; it is not intended for intraoral use. It is a rod-like device made of metal [e.g., titanium (Ti)]. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Secondary	04251574837462	GS1
Primary	EMKA02821ET9	HIBCC

Customer Contacts

• Phone: [phone]
• Email: [email protected]