Catalog Number

MC-2263

Brand Name

Medium Manual Percussor Cup

Version/Model Number

MC-2263

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"

Yes

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

GWZ

Product Code Name

Percussor

Public Device Record Key

1384e2b0-2fc9-4ead-a237-9eaf7367430e

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 11, 2017

Package DI Number

10858409005327

Quantity per Package

50

Contains DI Package

00858409005320

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case