FDA UDI In Commercial Distribution 🇺🇸 United States

EndyMed PRO MAX, FSR MAX Handpiece

DI: 07290016814439 · Model: FSR MAX Handpiece · ENDYMED MEDICAL LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EndyMed PRO MAX, FSR MAX Handpiece
Primary DI
07290016814439
Version / Model
FSR MAX Handpiece
Catalog Number
ND_PRD00471-00
Company Name
ENDYMED MEDICAL LTD
Labeler DUNS
531958689
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-16
Public Version
3
Public Version Date
2025-11-18
Public Version Status
Update
Public Device Record Key
bc781299-ac63-4bce-b6fd-696a19098e2d

Device Description

The handpiece is used as an accessory to EndyMed Pro MAX system, which is a noninvasive device intended for use in Dermatologic procedures. The FSR Max Handpiece is intended for dermatological procedures requiring ablation and resurfacing of the skin.

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
OUH Skin Resurfacing Rf Applicator

GMDN Terms

Code Name
44832 Multi-modality skin/body contouring system

Identifiers

Type ID
Primary 07290016814439

Customer Contacts