Focused Incisional Handpiece Set

GUDID 07290117771709

Direct Marking (DM): 07290117772102, 07290117772119, 07290117772133, 07290117772126.

LUMENIS BE LTD

Surgical laser system beam-focus handpiece
Primary Device ID07290117771709
NIH Device Record Keyca235754-9eac-4755-8f7b-cc98744a26f1
Commercial Distribution StatusIn Commercial Distribution
Brand NameFocused Incisional Handpiece Set
Version Model NumberNA
Company DUNS600763501
Company NameLUMENIS BE 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
GS107290117771709 [Primary]

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


[07290117771709]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-12-12
Device Publish Date2023-12-04

On-Brand Devices [Focused Incisional Handpiece Set]

07290117771709Direct Marking (DM): 07290117772102, 07290117772119, 07290117772133, 07290117772126.
07290117771693Direct Marking (DM): 07290117772102, 07290117772119, 07290117772133, 07290117772126.

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