Catalog Number

93192

Brand Name

Baha

Version/Model Number

93192

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

-

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

K945154

Product Code

FZE

Product Code Name

PROSTHESIS, NOSE, INTERNAL

Public Device Record Key

16834ddc-fabf-4f02-8f2c-81b79e6c4f21

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

June 07, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-