IM reamer head dove tail Ø13 x 27 mm, can. Ø3.1 mm - Intramedullary reamer head is used in combination - MPS Precimed SA

Duns Number:486741981

Device Description: Intramedullary reamer head is used in combination with the Intramedullary reamer shaft to Intramedullary reamer head is used in combination with the Intramedullary reamer shaft to ream the medullary cavity of long bones in traumatologic or limb lengthening surgery of the femur, tibia and humerus bones where medullary cavities need to be prepared prior to placing a nail.The intramedullary reamers are intended for use with a guide wire to permit to secure the assembly and a surgical drilling machine. A range of diameter is proposed in regards with the nail to be implanted. Different coupling are available to connect the shaft with existing power tool. The device is reusable.

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More Product Details

Catalog Number

T18373

Brand Name

IM reamer head dove tail Ø13 x 27 mm, can. Ø3.1 mm

Version/Model Number

T18373

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)

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

HTO

Product Code Name

Reamer

Device Record Status

Public Device Record Key

b46af58d-86e1-404d-b47f-56624bf2e4e4

Public Version Date

August 31, 2020

Public Version Number

1

DI Record Publish Date

August 21, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MPS PRECIMED SA" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 299