Coblation, TOPAZ Q6002-01

GUDID 00817470004373

TOPAZ EPF MICRODEBRIDER ICW

Smith & Nephew, Inc.

Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use Universal foot-controlled electrosurgical diathermy system conducting unit, single-use
Primary Device ID00817470004373
NIH Device Record Keyf52db06c-e129-4401-9f9b-711182226e26
Commercial Distribution StatusIn Commercial Distribution
Brand NameCoblation, TOPAZ
Version Model NumberQ6002-01
Catalog NumberQ6002-01
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 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)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)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)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)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)821-5700
Emailgudid@smith-nephew.com
Phone+1(800)821-5700
Emailgudid@smith-nephew.com
Phone+1(800)821-5700
Emailgudid@smith-nephew.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100817470004373 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

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

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.