Catalog Number

-

Brand Name

LOCalizer

Version/Model Number

HB110

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

PBY

Product Code Name

Temporary Tissue Marker

Public Device Record Key

6bb8e0dc-0bee-4f1a-aad8-964fe62e63ea

Public Version Date

June 10, 2022

Public Version Number

6

DI Record Publish Date

June 16, 2017

Package DI Number

10855436007010

Quantity per Package

5

Contains DI Package

00855436007013

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shelf Carton