Catalog Number

J-008.31.277

Brand Name

MICROLIGHT

Version/Model Number

J-008.31.277

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

EQH

Product Code Name

SOURCE, CARRIER, FIBEROPTIC LIGHT

Public Device Record Key

9d04ea6e-6a80-4f63-a95e-30b14052ad6e

Public Version Date

January 08, 2021

Public Version Number

2

DI Record Publish Date

September 17, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-