Catalog Number

-

Brand Name

BAHADIR USA

Version/Model Number

Y 843.09

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"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K131407

Product Code

FSM

Product Code Name

Tray, Surgical, Instrument

Public Device Record Key

d39c7fba-1316-41c5-9d49-d971528c2175

Public Version Date

September 16, 2022

Public Version Number

5

DI Record Publish Date

September 09, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-