Catalog Number

-

Brand Name

ELECTROSURGICAL SNARE

Version/Model Number

SD-7P-1

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 15, 2022

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

-

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

FAS

Product Code Name

ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL

Public Device Record Key

6a4b85ac-9538-4a6b-b16d-4c1690d2b50d

Public Version Date

August 16, 2022

Public Version Number

5

DI Record Publish Date

September 21, 2016

Package DI Number

14953170035965

Quantity per Package

1

Contains DI Package

04953170035968

Package Discontinue Date

August 15, 2022

Package Status

Not in Commercial Distribution

Package Type

-