Phoenix Thera-Lase system

GUDID 00860012325030

PHOENIX THERA-LASE SYSTEMS, LLC

Musculoskeletal/physical therapy laser, professional
Primary Device ID00860012325030
NIH Device Record Key60803ce3-e3a3-4e70-ac02-216d6c195cca
Commercial Distribution StatusIn Commercial Distribution
Brand NamePhoenix Thera-Lase system
Version Model Number70W
Company DUNS079869313
Company NamePHOENIX THERA-LASE SYSTEMS, LLC
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 Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100860012325030 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ILYLamp, Infrared, Therapeutic Heating

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-10-17
Device Publish Date2024-10-09

On-Brand Devices [Phoenix Thera-Lase system ]

0086001232502370W
0086001232501670W
0086001232500970W
0086001231099970W
0086001231098270W
0086001231097570W
0086001231096870W
0086001231095170W
0086001231094470W
0086001231093770W
0086001231092070W
0086001231091370W
0086001231090670W
0008600123250370W
0086001259492475W
0086001259491775W
0086001259490070W
0086001232509270W
0086001232508575W
0086001232507870W
0086001232505475W
0000861232504770W
0086001232503070W

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