DUO+ 240 Treatment Head

GUDID B271DUO2400

Meditech International Inc

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Primary Device IDB271DUO2400
NIH Device Record Key7a86046f-589a-4c0d-a35a-e968f7769251
Commercial Distribution StatusIn Commercial Distribution
Brand NameDUO+ 240 Treatment Head
Version Model NumberDUO+ 240
Company DUNS255079485
Company NameMeditech International Inc
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
HIBCCB271DUO2400 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ILYLamp, Infrared, Therapeutic Heating
NHNPowered Light Based Non-Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-08-09

On-Brand Devices [DUO+ 240 Treatment Head]

B271LSB3000P0DUO+ 240 Treatment Head (LS-B 3000+)
B271DUO2400DUO+ 240

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