FemiLift Hygienic, Single Use Probe ACCO17111377

GUDID 17290110121744

ALMA LASERS LTD.

Multi-modality skin surface treatment system
Primary Device ID17290110121744
NIH Device Record Key0548f7b2-351c-4f3f-a2e5-4e24d1bd7e89
Commercial Distribution StatusIn Commercial Distribution
Brand NameFemiLift Hygienic, Single Use Probe
Version Model Number1
Catalog NumberACCO17111377
Company DUNS532283264
Company NameALMA LASERS 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 Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS117290110121744 [Primary]
GS117290110121751 [Package]
Package: [6 Units]
In Commercial Distribution

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 Date2019-10-01
Device Publish Date2019-09-23

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07290110123444 - NIR Face (6) HP2024-02-07

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