Catalog Number

125-2235T

Brand Name

Epimed

Version/Model Number

125-2235T

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"

-

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

K030562,K030562

Product Code

BSP

Product Code Name

NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

Public Device Record Key

0b400b9b-5180-4de4-899a-3ef15ebc26fc

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

October 20, 2017

Package DI Number

10818788020854

Quantity per Package

10

Contains DI Package

00818788020857

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case