EndyMed PRO 85W System 220V ND_PRD00009_F

GUDID 07290016814187

The EndyMed Pro System is a noninvasive device intended for use in Dermatologic and General Surgical procedures for the non- invasive treatment of mil

ENDYMED MEDICAL LTD

Multi-modality skin contouring system
Primary Device ID07290016814187
NIH Device Record Key1c66ae89-3d57-46cd-955f-c5e9c52bb0cf
Commercial Distribution StatusIn Commercial Distribution
Brand NameEndyMed PRO 85W System 220V
Version Model NumberPRO 85W System 220V
Catalog NumberND_PRD00009_F
Company DUNS531958689
Company NameENDYMED MEDICAL LTD
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com
Phone1-855-363-9633
Emailservice@endymed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107290016814187 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-03-21
Device Publish Date2019-03-03

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