Catalog Number

Tumark-BREV-P-Q

Brand Name

Tumark® Professional Q for Brevera® Petite

Version/Model Number

Tumark-BREV-P-Q

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NEU

Product Code Name

Marker, Radiographic, Implantable

Public Device Record Key

91cd8256-4682-408c-a9bc-716b733ad586

Public Version Date

June 10, 2022

Public Version Number

3

DI Record Publish Date

November 26, 2018

Package DI Number

24250195611332

Quantity per Package

10

Contains DI Package

14250195611335

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-