EndyMed PRO MAX, Contour MAX Handpiece ND_PRD00467-00

GUDID 07290016814477

The EndyMed Contour Handpiece is intended for the treatment of the following medical conditions; using the Contour applicator for delivery of non-thermal RF combined with massage: • Relief of minor muscle aches and pain, relief of muscle spasm • Temporary improvement of local blood circulation • Temporary reduction in the appearance of cellulite.

ENDYMED MEDICAL LTD

Multi-modality skin contouring system
Primary Device ID07290016814477
NIH Device Record Keybb56dcfa-3831-4f26-9b5f-e4902b97cff4
Commercial Distribution Discontinuation2024-05-16
Commercial Distribution StatusNot in Commercial Distribution
Brand NameEndyMed PRO MAX, Contour MAX Handpiece
Version Model NumberContour MAX Handpiece
Catalog NumberND_PRD00467-00
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 Datefalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS107290016814477 [Primary]

FDA Product Code

PBXMassager, Vacuum, Radio Frequency Induced Heat

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-05-24
Device Publish Date2024-05-16

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