Catalog Number

E402

Brand Name

EXMOOR

Version/Model Number

E402

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

MXP

Product Code Name

Bone Particle Collector

Public Device Record Key

eec11a29-22f2-4fdf-8183-5c41293ed0de

Public Version Date

December 21, 2020

Public Version Number

2

DI Record Publish Date

September 11, 2018

Package DI Number

05060180251956

Quantity per Package

5

Contains DI Package

05060180256180

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

A BOX