Primary Device ID | 07290016814125 |
NIH Device Record Key | a9056635-353c-4cb7-a7aa-a481c6a860b7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EndyMed Pro FSR Handpiece |
Version Model Number | Pro FSR Handpiece |
Catalog Number | ND_PRD00013 |
Company DUNS | 531958689 |
Company Name | ENDYMED MEDICAL LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1-855-363-9633 |
service@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com | |
Phone | 1-855-363-9633 |
support@endymed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290016814125 [Primary] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
OUH | Skin Resurfacing Rf Applicator |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-03-21 |
Device Publish Date | 2018-12-31 |
07290016814668 - PURE DentA | 2024-11-14 The ENDYMED PURE DentA is a device intended for use in Dermatologic and General Surgical Procedures. |
07290016814408 - EndyMed PRO MAX, System, 110V | 2024-05-24 The EndyMed PRO MAX System is a noninvasive device intended for use in Dermatologic and General Surgical procedures for the non- |
07290016814415 - endyMed PRO MAX, Intensif MAX Handpiece | 2024-05-24 The Intensif applicator is intended for use in dermatologic and general surgical procedure for electrocoagulation nd hemostasis |
07290016814422 - EndyMed PRO MAX, Small MAX Handpiece | 2024-05-24 The handpiece is used as an accessory to EndyMed Pro MAX system, which is a noninvasive device intended for use in Dermatologic |
07290016814439 - EndyMed PRO MAX, FSR MAX Handpiece | 2024-05-24 The handpiece is used as an accessory to EndyMed Pro MAX system, which is a noninvasive device intended for use in Dermatologic |
07290016814446 - EndyMed PRO MAX, iFine MAX Handpiece | 2024-05-24 The handpiece is used as an accessory to EndyMed Pro MAX system, which is a noninvasive device intended for use in Dermatologic |
07290016814453 - EndyMed PRO MAX,Shaper MAX Handpiece | 2024-05-24 The handpiece is used as an accessory to EndyMed Pro MAX system, which is a noninvasive device intended for use in Dermatologic |
07290016814460 - EndyMed PRO MAX,Mini Shaper MAX Handpiece | 2024-05-24 The handpiece is used as an accessory to EndyMed PRO MAX system, which is a noninvasive device intended for use in Dermatologi |