210266

GUDID 03596010448262

RAKE RETRACTOR 60.3 WIDEX50.8 DEEP 215.9 OVERALL

Smith & Nephew, Inc.

Orthopaedic retractor
Primary Device ID03596010448262
NIH Device Record Key5a7cee8d-a3b7-4298-bcfb-4d6f187f5364
Commercial Distribution StatusIn Commercial Distribution
Version Model Number210266
Catalog Number210266
Company DUNS109903521
Company NameSmith & Nephew, Inc.
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS103596010448262 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HSDPROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


[03596010448262]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2021-10-11
Device Publish Date2015-09-28

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