LS-6000

GUDID B108043PO30WMUS00

BTL INDUSTRIES LIMITED

Red-light phototherapy unit, professional
Primary Device IDB108043PO30WMUS00
NIH Device Record Key899d7467-08a2-4e0b-abbd-57d5230cd5c3
Commercial Distribution StatusIn Commercial Distribution
Brand NameLS-6000
Version Model NumberLS-6000
Company DUNS733532951
Company NameBTL INDUSTRIES LIMITED
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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB108043PO30WMUS00 [Primary]

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 Date2024-04-01
Device Publish Date2024-03-22

Devices Manufactured by BTL INDUSTRIES LIMITED

B108699BELTMEU00 - Belt2024-11-14
B108699HEADRESTMEU00 - Headrest2024-11-14
B108899PO11C1ENUS0150 - EMSCULPT NEO2024-10-01
B108699APM2MUS00 - EXOMIND applicator2024-09-05
B108699PO2M2MUS00 - EXOMIND2024-09-05
B108043PO30WMUS00 - LS-60002024-04-01
B108043PO30WMUS00 - LS-60002024-04-01
B108451POSCAEL2MUS00 - Scanning System for LS-60002024-04-01
B108899AP2C2MUS20 - Small applicator2023-12-18

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.