Catalog Number

-

Brand Name

M300 Series (ceiling, Mobile)

Version/Model Number

M310

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FTD

Product Code Name

Lamp, Surgical

Public Device Record Key

9955972c-4e80-45a4-bea5-6dbc2ca19b6f

Public Version Date

May 26, 2021

Public Version Number

5

DI Record Publish Date

August 28, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-