Catalog Number

M50784

Brand Name

Ponto

Version/Model Number

M50784

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 30, 2016

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

MAH

Product Code Name

Hearing Aid, Bone Conduction, Implanted

Public Device Record Key

d525b228-e36d-4dee-89a6-425f5d8a4a17

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 10, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-