Lumenis Pulse 30H GA-2003322D

GUDID 07290109147390

LUMENIS LTD.

General/multiple surgical solid-state laser system General/multiple surgical solid-state laser system General/multiple surgical solid-state laser system General/multiple surgical solid-state laser system General/multiple surgical solid-state laser system General/multiple surgical solid-state laser system General/multiple surgical solid-state laser system General/multiple surgical solid-state laser system General/multiple surgical solid-state laser system General/multiple surgical solid-state laser system General/multiple surgical solid-state laser system

Primary Device ID	07290109147390
NIH Device Record Key	25464c7c-44bc-4a2b-abda-fc18741fb8d5
Commercial Distribution Status	In Commercial Distribution
Brand Name	Lumenis Pulse 30H
Version Model Number	Lumenis Pulse 30H
Catalog Number	GA-2003322D
Company DUNS	600166524
Company Name	LUMENIS LTD.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	false
Serial Number	true
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290109147390 [Primary]

FDA Product Code

GEX	Powered Laser Surgical Instrument

Sterilization

Steralize Prior To Use	false
Device Is Sterile	false

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2022-09-27
Device Publish Date	2022-09-19

On-Brand Devices [Lumenis Pulse 30H]

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