SPEEDHIP 23-2014

GUDID 00817470012255

INLINE REUSABLE DRILL GUIDE SPEEDHIP

Smith & Nephew, Inc.

Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable
Primary Device ID00817470012255
NIH Device Record Keyd785d039-43c4-4bb9-9585-c846627b8e09
Commercial Distribution Discontinuation2018-08-31
Commercial Distribution StatusNot in Commercial Distribution
Brand NameSPEEDHIP
Version Model Number23-2014
Catalog Number23-2014
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 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

Device Identifiers

Device Issuing AgencyDevice ID
GS100817470012255 [Primary]

FDA Product Code

HXYBRACE, DRILL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00817470012255]

Moist Heat or Steam Sterilization


[00817470012255]

Moist Heat or Steam Sterilization


[00817470012255]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-11-22
Device Publish Date2018-05-21

On-Brand Devices [SPEEDHIP]

00817470012255INLINE REUSABLE DRILL GUIDE SPEEDHIP
00817470012248INLINE REUSABLE OBTURATOR SPEEDHIP
00885556724590INLINE REUSABLE DRILL GUIDE SPEEDHIP
00885556724583INLINE REUSABLE OBTURATOR SPEEDHIP
00885556724576INLINE REUSABLE DRILL SPEEDHIP

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