FDA UDI Not in Commercial Distribution 🇺🇸 United States

EndyMed PRO 85W System Face 220V

DI: 07290016814224 · Model: PRO 85W System Face 220V · ENDYMED MEDICAL LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EndyMed PRO 85W System Face 220V
Primary DI
07290016814224
Version / Model
PRO 85W System Face 220V
Catalog Number
ND_PRD00009_F_F
Company Name
ENDYMED MEDICAL LTD
Labeler DUNS
531958689
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-03
Public Version
3
Public Version Date
2023-06-26
Public Version Status
Update
Public Device Record Key
ba39be3f-c686-46bc-a416-6744d024bea8
Distribution End Date
2023-06-25

Device Description

The EndyMed Pro System is a noninvasive device intended for use in Dermatologic and General Surgical procedures for the non- invasive treatment of mild to moderate facial wrinkles and rhytides

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
No
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
44832 Multi-modality skin contouring system

Identifiers

Type ID
Primary 07290016814224

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K083461 000