NA - 1.0MM X 14IN NITINOL GUIDE WIRE - STRYKER CORPORATION

Duns Number:187502109

Device Description: 1.0MM X 14IN NITINOL GUIDE WIRE

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More Product Details

Catalog Number

234-030-027

Brand Name

NA

Version/Model Number

234-030-027

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

NBH

Product Code Name

ACCESSORIES,ARTHROSCOPIC

Device Record Status

Public Device Record Key

2e4c8da1-3caf-464e-afc3-a27abb880ee3

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 09, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"STRYKER CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 2188
2 A medical device with a moderate to high risk that requires special controls. 3183
U Unclassified 60