Catalog Number

ME725M1T

Brand Name

Megadyne

Version/Model Number

ME725M1T

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

K200253,K200253,K200253

Product Code

GEI

Product Code Name

Electrosurgical, cutting & coagulation & accessories

Public Device Record Key

7b9ffec6-2530-4963-84c3-ff7624ee606c

Public Version Date

June 11, 2021

Public Version Number

6

DI Record Publish Date

August 03, 2020

Package DI Number

50614559105946

Quantity per Package

60

Contains DI Package

10614559105948

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE