TWINFIX - TWINFIX TI 5.0 QUICK-T (TICRON) - Smith & Nephew, Inc.

Duns Number:109903521

Device Description: TWINFIX TI 5.0 QUICK-T (TICRON)

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


More Product Details

Catalog Number

72200767

Brand Name

TWINFIX

Version/Model Number

72200767

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 17, 2022

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

JDR

Product Code Name

STAPLE, FIXATION, BONE

Device Record Status

Public Device Record Key

a400e74e-e8e1-4518-83aa-56e10ef68dc3

Public Version Date

March 18, 2022

Public Version Number

6

DI Record Publish Date

August 29, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"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