Pistol.Long

GUDID 14897076721860

TENS PLUS INDUSTRIAL COMPANY

Cupping therapy device
Primary Device ID14897076721860
NIH Device Record Key9e719375-04e7-4a46-bf52-b3a6208418e2
Commercial Distribution StatusIn Commercial Distribution
Brand NamePistol.Long
Version Model NumberDY2111
Company DUNS663211978
Company NameTENS PLUS INDUSTRIAL COMPANY
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 Numberfalse
Manufacturing Datefalse
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
GS114897076721860 [Primary]

FDA Product Code

KNMDevice, Pressure Applying

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-13
Device Publish Date2023-06-05

Devices Manufactured by TENS PLUS INDUSTRIAL COMPANY

14897076721457 - Lion.Warm.XL2023-06-13
14897076721655 - Multi.D.1.52023-06-13
14897076721815 - Moxa.Bx.BamS2023-06-13
14897076721822 - Moxa.Bx.BamL2023-06-13
14897076721853 - Pistol2023-06-13
14897076721860 - Pistol.Long2023-06-13
14897076721860 - Pistol.Long2023-06-13
14897076721877 - Ins.MP.S2023-06-13
14897076721884 - Ins.MP.M2023-06-13

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