SLD+ 120 Treatment Head

GUDID B271SLD1200

Meditech International Inc

Red-light phototherapy unit, line-powered
Primary Device IDB271SLD1200
NIH Device Record Key8ef9ef11-ba82-4576-a44f-a905a34e5010
Commercial Distribution StatusIn Commercial Distribution
Brand NameSLD+ 120 Treatment Head
Version Model NumberSLD+ 120
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
HIBCCB271SLD1200 [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 StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-08-09

Devices Manufactured by Meditech International Inc

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B271CUPA0 - Arthritis Controller Unit2023-09-26
B271CU0 - CU Controller2018-07-06
B271CUP0 - CU+ Controller2018-07-06
B271DUO1800 - DUO+ 180 Treatment Head2018-07-06
B271DUO2400 - DUO+ 240 Treatment Head2018-07-06
B271LDI2000 - LD-I 200 Treatment Head2018-07-06

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