FDA UDI Not in Commercial Distribution 🇺🇸 United States

EndyMed Pure system 220V

DI: 07290016814286 · Model: Pure system 220V · ENDYMED MEDICAL LTD
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EndyMed Pure system 220V
Primary DI
07290016814286
Version / Model
Pure system 220V
Catalog Number
ND_PRD00077
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
8722d65e-28ac-4001-ae79-b3e8cfa0a392
Distribution End Date
2023-06-25

Device Description

The EndyMed Pure System is a noninvasive device intended for use in Dermatologic and General Surgical procedure.

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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
44832 Multi-modality skin contouring system

Identifiers

Type ID
Primary 07290016814286

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K120513 000