XLase Plus 1077USA

GUDID 00850033906004

BIOTEC ITALIA SRL

Light-energy skin surface treatment system applicator
Primary Device ID00850033906004
NIH Device Record Key04cfe8b8-b7aa-4eb8-9692-78fb88e1f927
Commercial Distribution StatusIn Commercial Distribution
Brand NameXLase Plus
Version Model Number1077USA
Catalog Number1077USA
Company DUNS541871273
Company NameBIOTEC ITALIA SRL
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
GS100850033906004 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

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 Date2024-08-06
Device Publish Date2024-07-29

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