Catalog Number

-

Brand Name

MAXUM

Version/Model Number

M220L

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

MRI safety Status

MR Unsafe

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

P010023

Product Code

MPV

Product Code Name

Implant, Hearing, Active, Middle Ear, Partially Implanted

Public Device Record Key

dab59744-21b8-42f8-be4b-0a8cc2476a06

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 03, 2014

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-