Midwest® E Plus - Midwest® E Plus 1:1 S - SIRONA Dental Systems GmbH

Duns Number:340306351

Device Description: Midwest® E Plus 1:1 S

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

-

Brand Name

Midwest® E Plus

Version/Model Number

875230

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

EGS

Product Code Name

Handpiece, Contra- And Right-Angle Attachment, Dental

Device Record Status

Public Device Record Key

e398e39d-a050-4718-91dd-4793091eb76c

Public Version Date

May 17, 2022

Public Version Number

5

DI Record Publish Date

February 09, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SIRONA DENTAL SYSTEMS GMBH" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 235
2 A medical device with a moderate to high risk that requires special controls. 326