Catalog Number

231-1810

Brand Name

Epimed

Version/Model Number

231-1810

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

K041021,K041021

Product Code

GXI

Product Code Name

Probe, radiofrequency lesion

Public Device Record Key

b4066f6f-7331-4daf-9a05-70bcd9a19e9d

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

June 04, 2020

Package DI Number

10818788023138

Quantity per Package

25

Contains DI Package

00818788023131

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case