Coblation, TOPAZ Q6003-01

GUDID 00817470004458

TOPAZ CANNULA OBTURATOR SY EPF

Smith & Nephew, Inc.

Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use
Primary Device ID00817470004458
NIH Device Record Key85b08b65-a0fd-49c1-a85c-6f0881716a8a
Commercial Distribution StatusIn Commercial Distribution
Brand NameCoblation, TOPAZ
Version Model NumberQ6003-01
Catalog NumberQ6003-01
Company DUNS109903521
Company NameSmith & Nephew, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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

Customer Support Contacts

Phone+1(800)821-5700
Emailgudid@smith-nephew.com
Phone+1(800)821-5700
Emailgudid@smith-nephew.com
Phone+1(800)821-5700
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
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100817470004458 [Primary]

FDA Product Code

GEACANNULA, SURGICAL, GENERAL & PLASTIC SURGERY

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-01-31
Device Publish Date2015-08-29

On-Brand Devices [Coblation, TOPAZ]

00817470004458TOPAZ CANNULA OBTURATOR SY EPF
00817470004380TOPAZ MICRODEBRIDER ICW
00817470004373TOPAZ EPF MICRODEBRIDER ICW

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