MEDI

Basic Information

• Brand Name: MEDI
• Primary DI: 00636257153451
• Version / Model: AK1L5W2
• Company Name: MEDI MANUFACTURING, INC.
• Labeler DUNS: 960754430
• Distribution Status: Not in Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2018-11-20
• Public Version: 4
• Public Version Date: 2021-11-23
• Public Version Status: Update
• Public Device Record Key: 7c9020ff-a856-4e68-9e0f-8e38eba9eca9
• Distribution End Date: 2020-04-20

Device Description

***DISC*20-30 STUMP SHRINKER AK 12" LONG

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: Yes
• 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
IPM	COVER, LIMB	Physical Medicine	890.3025	1

GMDN Terms

Code	Name	Definition	Implantable	Status
43222	Limb-worn device hygienic cover	A device made of fabric or harder materials designed to cover an external prosthetic or orthotic device worn on a limb (e.g., cast, foot orthosis), or an external fixation system for a limb, primarily to function as a hygienic barrier to protect the device and patient from contamination; it is not intended to be applied directly to the limb for a therapeutic purpose. This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00636257153451	GS1

Customer Contacts

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