390-0224

GUDID 00886385022338

Sigmoid Notch Screw

Stryker Trauma SA

Wrist ulna-head prosthesis
Primary Device ID00886385022338
NIH Device Record Key7f60f129-f769-4b5e-bee0-b55cfaea712e
Commercial Distribution StatusIn Commercial Distribution
Version Model Number390-0224
Catalog Number390-0224
Company DUNS481999654
Company NameStryker Trauma SA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Length26 Millimeter
Length26 Millimeter
Length26 Millimeter
Length26 Millimeter
Length26 Millimeter
Length26 Millimeter
Length26 Millimeter
Length26 Millimeter
Length26 Millimeter
Length26 Millimeter
Length26 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100886385022338 [Primary]

FDA Product Code

KXEPROSTHESIS, WRIST, HEMI-, ULNAR

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2015-09-24

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