Catalog Number

-

Brand Name

Lumos Surgical Light Series

Version/Model Number

Lumos L5

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

FSS

Product Code Name

Light, Surgical, Floor Standing

Public Device Record Key

78fa43a4-8a14-4ad0-8ec4-875dcab5aa3b

Public Version Date

February 23, 2022

Public Version Number

1

DI Record Publish Date

February 15, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-