Moses™ 365 D\F\L

GUDID 07290109143408

LUMENIS LTD.

Tissue morcellation system
Primary Device ID07290109143408
NIH Device Record Key32cc88d9-3efa-4bfb-b915-76131a4b9492
Commercial Distribution StatusIn Commercial Distribution
Brand NameMoses™ 365 D\F\L
Version Model NumberMoses™ 365 D\F\L
Company DUNS600166524
Company NameLUMENIS 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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx

Device Identifiers

Device Issuing AgencyDevice ID
GS107290109143408 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-11-02

Devices Manufactured by LUMENIS LTD.

07290118853701 - Lumenis Pulse 60H, 60Hz2023-12-18
07290109144924 - Stellar SapphireCool LG 6mm2023-08-16
07290109144931 - Stellar SapphireCool LG 15x352023-08-16
07290109144948 - Stellar SapphireCool LG 8x152023-08-16
07290109146676 - SurgiTouch Scanner 2022-09-30
07290109146133 - UltraPulse® DUO2022-09-28 UltraPulse DUO
07290109147055 - VersaPulse PowerSuite 80/100W2022-09-27
07290109147062 - VersaPulse PowerSuite 80/100W2022-09-27

Trademark Results [Moses]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MOSES
MOSES
90229308 not registered Live/Pending
KAIROS IoT WATER CONTROLS, LLC
2020-10-01
MOSES
MOSES
88682696 not registered Live/Pending
Lumenis Ltd.
2019-11-06
MOSES
MOSES
87687442 5778537 Live/Registered
LUMENIS LTD.
2017-11-16
MOSES
MOSES
87676285 not registered Dead/Abandoned
LUMENIS LTD.
2017-11-08
MOSES
MOSES
87225148 not registered Dead/Abandoned
Sight and Sound Ministries, Inc.
2016-11-03
MOSES
MOSES
87178567 5874646 Live/Registered
Knowledge Works NY Inc.
2016-09-21
MOSES
MOSES
87053350 not registered Dead/Abandoned
Chaonan Feng
2016-05-28
MOSES
MOSES
86645944 not registered Dead/Abandoned
Chaonan Feng
2015-05-29
MOSES
MOSES
86618198 5672058 Live/Registered
Gurt, Sarah
2015-05-04
MOSES
MOSES
86618198 5672058 Live/Registered
FREEDOM MOSES LLC
2015-05-04
MOSES
MOSES
85746976 4349652 Live/Registered
Mozafar M. Somekhian
2012-10-05
MOSES
MOSES
78301146 not registered Dead/Abandoned
Trio, Inc.
2003-09-16

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.