Lumenis Pulse 30H GA-2003322D

GUDID 07290109147390

LUMENIS LTD.

General/multiple surgical solid-state laser system
Primary Device ID07290109147390
NIH Device Record Key25464c7c-44bc-4a2b-abda-fc18741fb8d5
Commercial Distribution StatusIn Commercial Distribution
Brand NameLumenis Pulse 30H
Version Model NumberLumenis Pulse 30H
Catalog NumberGA-2003322D
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

Device Identifiers

Device Issuing AgencyDevice ID
GS107290109147390 [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 [Lumenis Pulse 30H]

07290109140698Lumenis Pulse 30H
07290109145990Lumenis Pulse 30H
07290109145983Lumenis Pulse 30H
07290109147390Lumenis Pulse 30H
07290109147314Lumenis Pulse 30H

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