Dermapac, Inc.

Basic Information

• Brand Name: Dermapac, Inc.
• Primary DI: 10810102270976
• Version / Model: 7106
• Company Name: Dermapac Inc.
• Labeler DUNS: 796088466
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 25
• Record Status: Published
• Publish Date: 2022-09-12
• Public Version: 1
• Public Version Date: 2022-09-20
• Public Version Status: New
• Public Device Record Key: dae6e930-628d-4aef-86df-708700e0eaa5

Device Description

3/16" Latex Free Rubber Bands 10/pk

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• 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: No
• Has Manufacturing Date: No
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: Yes
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
ECI	Band, Elastic, Orthodontic	Dental	872.5410	1

GMDN Terms

Code	Name	Definition	Implantable	Status
45148	Dental/maxillofacial surgical procedure kit, non-medicated, single-use	A collection of various sterile 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 single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Unit of Use	00810102270979	GS1
Primary	10810102270976	GS1

Customer Contacts

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