Lumenis Pulse 120H

GUDID 07290109140513

LUMENIS LTD.

General/multiple surgical solid-state laser system
Primary Device ID07290109140513
NIH Device Record Key1b50d50a-ffa0-4b2f-9864-346c62eae3c9
Commercial Distribution StatusIn Commercial Distribution
Brand NameLumenis Pulse 120H
Version Model NumberLumenis Pulse 120H
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

Device Identifiers

Device Issuing AgencyDevice ID
GS107290109140513 [Primary]

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-02-15
Device Publish Date2016-08-23

On-Brand Devices [Lumenis Pulse 120H]

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07290109145518Lumenis Pulse P120 30 Amp
07290109145501Lumenis Pulse 120H
07290109145495Lumenis Pulse 120H
07290109145488Lumenis Pulse 120H
07290109145464Lumenis Pulse 120H
07290109145457Lumenis Pulse 120H
07290109145440Lumenis Pulse 120H
07290109145433Lumenis Pulse 120H
07290109145426Lumenis Pulse 120H
07290109145419Lumenis Pulse 120H
07290109145402Lumenis Pulse 120H
07290109145150Lumenis Pulse Moses 2.0(INT)

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