mahe medical GmbH - K-Wire w. trocar/round end - mahe medical gmbh

Duns Number:342243334

Device Description: K-Wire w. trocar/round end _x000D_1.57mm/127mm, 6 pcs./unit _x0 K-Wire w. trocar/round end _x000D_1.57mm/127mm, 6 pcs./unit _x000D_

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More Product Details

Catalog Number

-

Brand Name

mahe medical GmbH

Version/Model Number

KM71-175

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

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

-

Product Code Details

Product Code

HTY

Product Code Name

PIN, FIXATION, SMOOTH

Device Record Status

Public Device Record Key

4b6c94d1-3d0d-4307-8942-1bf097e16ebc

Public Version Date

November 13, 2019

Public Version Number

1

DI Record Publish Date

November 05, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MAHE MEDICAL GMBH" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 19
2 A medical device with a moderate to high risk that requires special controls. 1976