Catalog Number

-

Brand Name

HAND SWITCH

Version/Model Number

U-HSCBM

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

April 11, 2022

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

MTX

Product Code Name

Microscope And Microscope Accessories, Reproduction, Assisted

Public Device Record Key

26ccc65b-e5e8-4655-b372-d5da26324d9d

Public Version Date

May 18, 2022

Public Version Number

2

DI Record Publish Date

September 21, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-