Electrical Extracorporeal Shock Wave Therapy Device

GUDID 06971410780278

Guangzhou Longest Science & Technology Co., Ltd.

Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system
Primary Device ID06971410780278
NIH Device Record Key68d730eb-f105-4eab-94b3-db1090f30324
Commercial Distribution StatusIn Commercial Distribution
Brand NameElectrical Extracorporeal Shock Wave Therapy Device
Version Model NumberLGT-2500S, config III
Company DUNS527141843
Company NameGuangzhou Longest Science & Technology Co., Ltd.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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
GS106971410780278 [Primary]

FDA Product Code

ISAMassager, Therapeutic, Electric

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-23
Device Publish Date2020-10-15

On-Brand Devices [Electrical Extracorporeal Shock Wave Therapy Device]

06971410780278LGT-2500S, config III
06971410780261LGT-2500S, config II

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