Nasal probe Starter Kit

GUDID 07290109141312

Additional DM DIs: 07290109144337 07290109144344 07290109144351 07290109144368 07290109144375 07290109144382 07290109144399 07290109144405 07290109144412

LUMENIS LTD.

General/multiple surgical solid-state/carbon dioxide laser system
Primary Device ID07290109141312
NIH Device Record Key0f1abed6-1313-477b-babd-e8c9b14e0980
Commercial Distribution StatusIn Commercial Distribution
Brand NameNasal probe Starter Kit
Version Model Number14630
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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
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
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx
Phone408-764-3000
Emailxxx@xxx.xxx

Device Identifiers

Device Issuing AgencyDevice ID
GS107290109141312 [Primary]
GS107290109144320 [Direct Marking]

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


[07290109141312]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-04-29
Device Publish Date2016-08-25

Devices Manufactured by LUMENIS LTD.

07290109147161 - Lumenis Pulse 120H2025-02-26
07290109147178 - Lumenis Pulse 120H2025-02-26
07290109147185 - Lumenis Pulse, Moses 2.0 (DOM)2025-02-26
07290109147192 - Lumenis Pulse 120H2025-02-26
07290109147208 - Lumenis Pulse, Moses 2.0 (INT)2025-02-26
07290109147215 - Lumenis Pulse 120H2025-02-26
07290109147222 - Lumenis Pulse 120H2025-02-26
07290109147291 - Lumenis Pulse 120H2025-02-26

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