Catalog Number

-

Brand Name

Zimmer Tourniquet

Version/Model Number

RM-60707500500

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KCY

Product Code Name

Tourniquet, Pneumatic

Public Device Record Key

346d10da-dac4-4b9c-8dc5-a61ff3be2cdb

Public Version Date

August 02, 2019

Public Version Number

3

DI Record Publish Date

June 16, 2017

Package DI Number

10816317023338

Quantity per Package

10

Contains DI Package

00816317023331

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case