Fizimed

Basic Information

• Brand Name: Fizimed
• Primary DI: 03770011873005
• Version / Model: Emy V1
• Company Name: FIZIMED
• Labeler DUNS: 269584479
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2022-05-16
• Public Version: 1
• Public Version Date: 2022-05-24
• Public Version Status: New
• Public Device Record Key: 4cb36411-ca1b-44b5-98ca-82dbeb03c72a

Device Characteristics

• Single Use: No
• 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: Yes
• 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
KXQ	Vibrator For Therapeutic Use, Genital	Obstetrics/Gynecology	884.5960	2

GMDN Terms

Code	Name	Definition	Implantable	Status
32686	Perineometer	A device consisting of a fluid-filled sack for intravaginal use that is attached to an external manometer. The device measures the strength of the perineal muscles by offering resistance to a patient's voluntary contractions of these muscles and is used to diagnose and to correct, through exercise, urinary incontinence or sexual dysfunction.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	03770011873005	GS1