NA - STEINMANN PIN DIAMOND POINT BOTH - Smith & Nephew, Inc.

Duns Number:109903521

Device Description: STEINMANN PIN DIAMOND POINT BOTH ENDS 9/64 X 9

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More Product Details

Catalog Number

128121

Brand Name

NA

Version/Model Number

128121

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)

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

HTY

Product Code Name

PIN, FIXATION, SMOOTH

Device Record Status

Public Device Record Key

0bfe9309-43e2-4532-b9b6-bdec01d8955a

Public Version Date

October 22, 2020

Public Version Number

3

DI Record Publish Date

August 29, 2015

Additional Identifiers

Package DI Number

23596010083023

Quantity per Package

6

Contains DI Package

03596010083029

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BX

"SMITH & NEPHEW, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 10651
2 A medical device with a moderate to high risk that requires special controls. 35590
3 A medical device with high risk that requires premarket approval 351