Midmark - The M9 Steam Sterilizer can be used in medical - MIDMARK CORPORATION

Duns Number:005036025

Device Description: The M9 Steam Sterilizer can be used in medical and dental offices, hospitals, clinics,nurs The M9 Steam Sterilizer can be used in medical and dental offices, hospitals, clinics,nursing homes, laboratories, and other facilities to sterilize heat and moisture stable reusable items (including dental handpieces) that are compatible with steam sterilization.The Midmark Data Logger is designed to connect with a Midmark sterilizer and electronically store sterilizer cycle data such as: sterilizer serial number, date and time the cycle was run, sterilization cycle parameters, errors and the cycle approving authority.

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More Product Details

Catalog Number

M9-040-DL

Brand Name

Midmark

Version/Model Number

M9-040 / 9A682001

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K163337

Product Code Details

Product Code

FLE

Product Code Name

Sterilizer, steam

Device Record Status

Public Device Record Key

ee146fbf-e26c-40db-8e83-45bdaafa4fab

Public Version Date

August 05, 2020

Public Version Number

1

DI Record Publish Date

July 28, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MIDMARK CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 838
2 A medical device with a moderate to high risk that requires special controls. 544