SurgiTouch Scanning Handpiece 260mm

GUDID 07290109141497

Additional DM UDI: 07290109144054; 07290109144061

LUMENIS LTD.

General/multiple surgical solid-state/carbon dioxide laser system
Primary Device ID07290109141497
NIH Device Record Key61d714d6-cb4b-4d81-806e-a0cbbf0099db
Commercial Distribution StatusIn Commercial Distribution
Brand NameSurgiTouch Scanning Handpiece 260mm
Version Model NumberSurgiTouch Scanning Handpiece 260mm
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

Device Identifiers

Device Issuing AgencyDevice ID
GS107290109141497 [Primary]
GS107290109144047 [Direct Marking]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


[07290109141497]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-02-27
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

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