Lumenis Pulse 60H, 50Hz GA-2006378D

GUDID 07290109147321

LUMENIS LTD.

General/multiple surgical solid-state laser system
Primary Device ID07290109147321
NIH Device Record Keyd248897e-b8b7-407a-b8c7-b10fa75075cb
Commercial Distribution StatusIn Commercial Distribution
Brand NameLumenis Pulse 60H, 50Hz
Version Model NumberLumenis Pulse 60H, 50Hz
Catalog NumberGA-2006378D
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
GS107290109147321 [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 60H, 50Hz]

07290109144665Lumenis Pulse 60H, 50Hz
07290109147321Lumenis Pulse 60H, 50Hz

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.