SPEEDSTITCH OM-8850

GUDID 00817470005929

SPEEDSTITCH NEEDLE

Smith & Nephew, Inc.

Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable Suturing unit, reusable
Primary Device ID00817470005929
NIH Device Record Key152d7666-15d0-4c70-9396-42db5c4eeba8
Commercial Distribution StatusIn Commercial Distribution
Brand NameSPEEDSTITCH
Version Model NumberOM-8850
Catalog NumberOM-8850
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 Latextrue
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
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
GS100817470005929 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GATSUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2020-02-06
Device Publish Date2017-11-13

On-Brand Devices [SPEEDSTITCH]

00817470005929SPEEDSTITCH NEEDLE
00817470001402SPEEDSTITCH DEVICE

Trademark Results [SPEEDSTITCH]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SPEEDSTITCH
SPEEDSTITCH
78294825 3096349 Dead/Cancelled
ARTHROCARE CORPORATION
2003-09-02

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