SurgiTouch Scanner AC-20007750D

GUDID 07290109147345

LUMENIS LTD.

General/multiple surgical solid-state/carbon dioxide laser system
Primary Device ID07290109147345
NIH Device Record Key259239bf-883b-415a-bb80-045e37ccfa4f
Commercial Distribution StatusIn Commercial Distribution
Brand NameSurgiTouch Scanner
Version Model Numberkit for UltraPulse/UltraPulse DUO
Catalog NumberAC-20007750D
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 Kittrue
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

Device Identifiers

Device Issuing AgencyDevice ID
GS107290109147345 [Primary]

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-09-27
Device Publish Date2022-09-19

On-Brand Devices [SurgiTouch Scanner]

07290109146720Upgrade kit for AcuPulse 30/40 to 30/40 ST
07290109147345kit for UltraPulse/UltraPulse DUO
07290109146676SurgiTouch Scanner

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