Catalog Number

-

Brand Name

seemann

Version/Model Number

ST-99-512

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

-

Product Code

GEI

Product Code Name

Electrosurgical, Cutting & Coagulation & Accessories

Public Device Record Key

6a9a3a5d-39f1-436f-a2fe-4e7e70b1057c

Public Version Date

February 07, 2019

Public Version Number

3

DI Record Publish Date

December 13, 2017

Package DI Number

26939029816652

Quantity per Package

20

Contains DI Package

16939029816655

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton Box