Catalog Number

-

Brand Name

EchoBlock MSK

Version/Model Number

EBA-2250

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

K063380,K063380

Product Code

BSP

Product Code Name

Needle, Conduction, Anesthetic (W/Wo Introducer)

Public Device Record Key

bf2cc8eb-b772-461a-ae7a-d52ec3e2751e

Public Version Date

June 03, 2022

Public Version Number

4

DI Record Publish Date

September 23, 2016

Package DI Number

14526737170739

Quantity per Package

25

Contains DI Package

04526737170732

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-