Catalog Number

271590

Brand Name

Tumark Vision

Version/Model Number

271590

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

42c0b65c-0616-4e3c-9705-05a3665c8e88

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

November 25, 2016

Package DI Number

04250195607843

Quantity per Package

10

Contains DI Package

04250195607836

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-