Primary Device ID | 07290109950013 |
NIH Device Record Key | 73f5a32f-33af-498d-a449-cfafe6076603 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | eMax |
Version Model Number | AS10812 |
Catalog Number | AS10812 |
Company DUNS | 532685716 |
Company Name | SYNERON 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 | false |
OTC Over-The-Counter | false |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com | |
Phone | 1.866.259.6661 |
info@Syneron-Candela.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290109950013 [Primary] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-20 |
07290109952703 - SA Flat Lrg. Repl. Cover 25x50mm, 4Hr, Velashape III | 2020-03-31 SA Flat Lrg. Repl. Cover 25x50mm, 4Hr, Velashape III |
07290109952857 - Intima Sterile 2 Internal + 1 External HP, Accessories Kit | 2020-02-10 Intima Sterile 2 Internal + 1 External HP, Accessories Kit |
07290109952864 - eTwo System | 2020-02-10 eTwo System |
17290109952724 - Regular Internal Handpiece 5-Pack Sterile Single-Use, CO2RE Intima | 2020-02-10 Regular Internal Handpiece 5-Pack Sterile Single-Use, CO2RE Intima |
17290109952823 - External Handpiece 5-Pack Sterile Single-Use, CO2RE Intima | 2020-02-10 External Handpiece 5-Pack Sterile Single-Use, CO2RE Intima |
17290109950379 - Internal, CO2RE Intima | 2019-02-07 Internal, CO2RE Intima |
07290109950167 - Purple swivel lens | 2019-02-07 Purple swivel lens |
07290109950273 - Lens, Gold & Silver | 2019-02-07 Lens, Gold & Silver Assy, CO2RE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EMAX 97185546 not registered Live/Pending |
eMax Holdings, LLC 2021-12-22 |
EMAX 97185517 not registered Live/Pending |
eMax Holdings, LLC 2021-12-22 |
EMAX 97105469 not registered Live/Pending |
MAXIN SMART MANUFACTURING CO., LTD. 2021-11-02 |
EMAX 90602005 not registered Live/Pending |
Sigma Powertrain, Inc. 2021-03-25 |
EMAX 90079008 not registered Live/Pending |
Encompass Group, LLC 2020-07-28 |
EMAX 87524764 not registered Dead/Abandoned |
303 Management, Inc. 2017-07-12 |
EMAX 86958875 not registered Dead/Abandoned |
YINYAN TECH US INC. 2016-03-30 |
EMAX 86935563 5121123 Live/Registered |
Mewah Brands (S) Pte Ltd 2016-03-10 |
EMAX 86175593 not registered Dead/Abandoned |
Farid, Tariq 2014-01-27 |
EMAX 85967327 not registered Dead/Abandoned |
United States Global Trading Services LLC 2013-06-22 |
EMAX 85249892 4028598 Live/Registered |
E-ONE, Inc. 2011-02-23 |
EMAX 85246183 4026089 Live/Registered |
E-ONE, Inc. 2011-02-18 |