Surgery set CERALOG® PROGRESSIVE-LINE Flex

Basic Information

• Brand Name: Surgery set CERALOG® PROGRESSIVE-LINE Flex
• Primary DI: E219H530000701
• Version / Model: H5300.0070
• Catalog Number: H5300.0070
• Company Name: ALTATEC GmbH
• Labeler DUNS: 322018193
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2023-12-19
• Public Version: 1
• Public Version Date: 2023-12-27
• Public Version Status: New
• Public Device Record Key: de7d3af6-556c-4cef-89e1-4e8d74a72f6e

Device Description

Surgery set CERALOG® PROGRESSIVE-LINE Flex

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: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: Yes
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: Yes
• Sterilization Methods: Moist Heat or Steam Sterilization

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
EJL	Bur, Dental	Dental	872.3240	1

GMDN Terms

Code	Name	Definition	Implantable	Status
45147	Dental/maxillofacial surgical procedure kit, non-medicated, reusable	A collection of various dental/surgical instruments, dressings and the necessary materials intended to be used to perform a dental or oral/maxillofacial surgical procedure. It does not contain any pharmaceuticals. This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	E219H530000701	HIBCC

Customer Contacts

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