UltraScan™ CPG

GUDID 07290109141657

Additional DM UDI: 07290109144252

LUMENIS LTD.

General/multiple surgical solid-state/carbon dioxide laser system
Primary Device ID07290109141657
NIH Device Record Keybd551a86-ffb0-435f-9554-f106c3be45b6
Commercial Distribution StatusIn Commercial Distribution
Brand NameUltraScan™ CPG
Version Model NumberUltraScan™ CPG
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 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

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

Device Identifiers

Device Issuing AgencyDevice ID
GS107290109141657 [Primary]
GS107290109144245 [Direct Marking]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


[07290109141657]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-11-08
Device Publish Date2016-08-28

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 [UltraScan]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ULTRASCAN
ULTRASCAN
88728148 not registered Live/Pending
Medical Positioning, Inc.
2019-12-16
ULTRASCAN
ULTRASCAN
86135554 4565650 Live/Registered
Heartweb Pty Ltd
2013-12-05
ULTRASCAN
ULTRASCAN
79053390 not registered Dead/Abandoned
Clipsal Australia Pty Ltd
2008-04-15
ULTRASCAN
ULTRASCAN
78425124 3419770 Live/Registered
PII Limited
2004-05-26
ULTRASCAN
ULTRASCAN
76542663 2923987 Live/Registered
LA-CO INDUSTRIES, INC.
2003-08-25
ULTRASCAN
ULTRASCAN
76380733 2787272 Live/Registered
Core Laboratories Global N. V.
2002-03-08
ULTRASCAN
ULTRASCAN
76233010 not registered Dead/Abandoned
PII Group Limited
2001-03-28
ULTRASCAN
ULTRASCAN
75643631 2523089 Live/Registered
GATAN, INC.
1999-02-19
ULTRASCAN
ULTRASCAN
75440575 not registered Dead/Abandoned
ICO P&O, INC.
1998-02-25
ULTRASCAN
ULTRASCAN
75440402 not registered Dead/Abandoned
ICO, Inc.
1998-02-25
ULTRASCAN
ULTRASCAN
75325581 not registered Dead/Abandoned
Krautkramer-Branson, Incorporated
1997-07-16
ULTRASCAN
ULTRASCAN
75139655 not registered Dead/Abandoned
ICO, Inc.
1996-07-25

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