BioMotion Cannulated 1st MPJ Hemi System HM2300

GUDID 00885556821725

CANNULATED HEMI IMPLANT XLARGE (23MM)

Smith & Nephew, Inc.

Wrist ulna-head prosthesis Wrist ulna-head prosthesis Wrist ulna-head prosthesis Wrist ulna-head prosthesis Wrist ulna-head prosthesis Wrist ulna-head prosthesis Wrist ulna-head prosthesis Wrist ulna-head prosthesis Wrist ulna-head prosthesis Wrist ulna-head prosthesis Wrist ulna-head prosthesis Wrist ulna-head prosthesis Wrist ulna-head prosthesis Wrist ulna-head prosthesis
Primary Device ID00885556821725
NIH Device Record Keya479277e-6d10-4aef-9a9e-218000d81085
Commercial Distribution StatusIn Commercial Distribution
Brand NameBioMotion Cannulated 1st MPJ Hemi System
Version Model NumberHM2300
Catalog NumberHM2300
Company DUNS045483575
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 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

Device Identifiers

Device Issuing AgencyDevice ID
GS100885556821725 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWDPROSTHESIS, TOE, HEMI-, PHALANGEAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00885556821725]

Moist Heat or Steam Sterilization


[00885556821725]

Moist Heat or Steam Sterilization


[00885556821725]

Moist Heat or Steam Sterilization


[00885556821725]

Moist Heat or Steam Sterilization


[00885556821725]

Moist Heat or Steam Sterilization


[00885556821725]

Moist Heat or Steam Sterilization


[00885556821725]

Moist Heat or Steam Sterilization


[00885556821725]

Moist Heat or Steam Sterilization


[00885556821725]

Moist Heat or Steam Sterilization


[00885556821725]

Moist Heat or Steam Sterilization


[00885556821725]

Moist Heat or Steam Sterilization


[00885556821725]

Moist Heat or Steam Sterilization


[00885556821725]

Moist Heat or Steam Sterilization


[00885556821725]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-09-07
Device Publish Date2022-12-21

On-Brand Devices [BioMotion Cannulated 1st MPJ Hemi System]

00885556821831HEMI GUIDE WIRE SMOOTH .062IN X 4IN
00885556821824HEMI STERILIZATION TRAY LID ONLY
00885556821817HEMI STERILIZATION TRAY
00885556821800BIOMOTION HEMI RASP
00885556821794CANNULATED HEMI SIZER XLARGE (23MM)
00885556821787CANNULATED HEMI SIZER LARGE (21MM)
00885556821770CANNULATED HEMI SIZER MEDIUM (19MM)
00885556821763CANNULATED HEMI SIZER SMALL (17MM)
00885556821756CANNULATED HEMI SIZER XSMALL (15MM)
00885556821749BIOMOTION SLIDE HAMMER
00885556821732BIOMOTION SLIDE BROACH
00885556821725CANNULATED HEMI IMPLANT XLARGE (23MM)
00885556821718CANNULATED HEMI IMPLANT LARGE (21MM)
00885556821701CANNULATED HEMI IMPLANT MEDIUM (19MM)
00885556821695CANNULATED HEMI IMPLANT SMALL (17MM)
00885556821688CANNULATED HEMI IMPLANT XSMALL (15MM)

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