LASERING SRL

GUDID 08056477090022

LASERING SRL

Dermatological solid-state laser system
Primary Device ID08056477090022
NIH Device Record Keyfd8fbe4b-706f-41b4-a9c6-c457feaa2ee2
Commercial Distribution StatusIn Commercial Distribution
Brand NameLASERING SRL
Version Model NumberVELURE S5
Company DUNS446096968
Company NameLASERING 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 Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108056477090022 [Primary]

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-02-06
Device Publish Date2018-06-07

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