Catalog Number

M1815

Brand Name

Achieve

Version/Model Number

M1815

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

NEU

Product Code Name

Marker, Radiographic, Implantable

Public Device Record Key

0be1e772-c752-4235-893a-fcab9b8e33bd

Public Version Date

June 10, 2022

Public Version Number

3

DI Record Publish Date

June 12, 2017

Package DI Number

50885403242371

Quantity per Package

5

Contains DI Package

10885403242373

Package Discontinue Date

-

Package Status

-

Package Type

Case