MEDI

Basic Information

• Brand Name: MEDI
• Primary DI: 04026398796086
• Version / Model: 64281
• Company Name: MEDI MANUFACTURING, INC.
• Labeler DUNS: 960754430
• Distribution Status: Not in Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2019-02-11
• Public Version: 3
• Public Version Date: 2022-06-10
• Public Version Status: Update
• Public Device Record Key: 1950ac43-8b93-488a-b3e3-fa6cbd6e30f7
• Distribution End Date: 2020-04-20

Device Description

***DISC*MANUMED ACTIVE WRIST LEFT SAND X

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• Over the Counter (OTC): Yes
• 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: Yes
• 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
ISZ	UNIT, WRIST, EXTERNAL LIMB COMPONENT, MECHANICAL	Physical Medicine	890.3420	1

GMDN Terms

Code	Name	Definition	Implantable	Status
41458	Wrist orthosis	A prefabricated (non-customized) externally applied orthopaedic appliance or apparatus designed to support, align, prevent, or correct deformities/injuries or to improve function of the wrist. This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	04026398796086	GS1

Customer Contacts

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