Catalog Number

-

Brand Name

THUNDERBEAT 5 mm,35 cm,Front-actuated Grip Type S

Version/Model Number

TB-0535FCS

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"

Yes

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

-

Product Code

GEI

Product Code Name

Electrosurgical, cutting & coagulation & accessories

Public Device Record Key

206e6e54-334f-455a-b074-ea8b158ca936

Public Version Date

June 21, 2022

Public Version Number

4

DI Record Publish Date

June 05, 2018

Package DI Number

14953170409674

Quantity per Package

5

Contains DI Package

04953170409677

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-