6900991

GUDID 00885554008784

SOD 2.9MM CANNULA W/DL INFLW

Smith & Nephew, Inc.

Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable Rigid endoscopic cannula, reusable
Primary Device ID00885554008784
NIH Device Record Keyd5990ba2-5603-4937-b5d5-cedb909b89a5
Commercial Distribution Discontinuation2017-04-04
Commercial Distribution StatusNot in Commercial Distribution
Version Model Number6900991
Catalog Number6900991
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100885554008784 [Primary]

FDA Product Code

KIJINSTRUMENT, SURGICAL, ORTHOPEDIC, DC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


[00885554008784]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2015-08-23

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00885556917978 - Legion2024-04-10 EM PROXIMAL GUIDE - L

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