Catalog Number

36.012.24SL

Brand Name

HF-knife 24CH Saline- resectoscopy electrotrode

Version/Model Number

36.012.24SL

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

FDC

Product Code Name

RESECTOSCOPE, WORKING ELEMENT

Public Device Record Key

555e377a-8015-4e67-8799-d1bc3f90979b

Public Version Date

June 05, 2020

Public Version Number

3

DI Record Publish Date

September 28, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-