JOURNEY II UNI 74036116

GUDID 00885556696422

RM/LL MODULAR SHIM UNCAPTURED

Smith & Nephew, Inc.

External orthopaedic fixation system, reusable
Primary Device ID00885556696422
NIH Device Record Key6dcbb0d7-a624-4079-9529-10268a55928e
Commercial Distribution StatusIn Commercial Distribution
Brand NameJOURNEY II UNI
Version Model Number74036116
Catalog Number74036116
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
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
GS100885556696422 [Primary]

FDA Product Code

FZXGuide, surgical, instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


[00885556696422]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-06-21
Device Publish Date2019-06-13

On-Brand Devices [JOURNEY II UNI]

00885556709702ANKLE CLAMP
00885556709696TIBIAL ALIGNMENT TUBE
00885556706787TIBIAL SHIM RM/LL - CAPTURED
00885556706770TIBIAL SHIM LM/RL - CAPTURED
00885556706763TIBIAL SHIM RM/LL - UNCAPTURED
00885556706756TIBIAL SHIM LM/RL - UNCAPTURED
00885556706749TIBIAL HEAD RM/LL
00885556706732TIBIAL HEAD LM/RL
00885556706725SPOON - 3MM
00885556706718SPOON - 2MM
00885556706701SPOON - 1MM
00885556706695CONNECTOR - 8MM
00885556706688ANKLE CLAMP
00885556706671TIBIAL ALIGNMENT TUBE
00885556696668NON ROTATING TIBIAL STYLUS 6MM / 8MM
00885556696651NON ROTATING TIBIAL STYLUS 2MM / 4MM
00885556686935UNI FEMORAL TRIAL IMPACTOR / HOLDER
00885556696569TIBIA CONNECTOR 8 MM CLOSED ALTERNATE
00885556696453LM/RL MODULAR SHIM CAPTURED
00885556696446LM/RL MODULAR SHIM UNCAPTURED
00885556696439RM/LL MODULAR SHIM CAPTURED
00885556696422RM/LL MODULAR SHIM UNCAPTURED
00885556696415RM/LL TIBIA RESECTION GUIDE ALTERNATE
00885556696408LM/RL TIBIA RESECTION GUIDE ALTERNATE
00885556696293FIXED ANKLE CLAMP
00885556692424JOURNEY II UNI LAT TIBIA INSERT TRIAL SZ 4-5 11MM
0088555669227117MM PIN - NON STERILE
00885556692264JOURNEY II UNI FEMORAL TRIAL HOLDER
00885556692257FEMORAL FREE IMPACTOR
008855566922403.5mm LOCKING HEX T-HANDLE
00885556692233FEMORAL PEG DRILL
00885556692226JOURNEY II UNI TIBIA SIZING HOOK
00885556692202TIBIA FREE IMPACTOR
00885556692196INSERT IMPLANT LOCKING TOOL
00885556692127KEEL PUNCH
00885556691946JOURNEY II UNI MED TIBIA INSERT TRIAL SZ 9-10 14MM
00885556691939JOURNEY II UNI MED TIBIA INSERT TRIAL SZ 9-10 13MM
00885556691922JOURNEY II UNI MED TIBIA INSERT TRIAL SZ 9-10 12MM
00885556691915JOURNEY II UNI MED TIBIA INSERT TRIAL SZ 9-10 11MM
00885556691908JOURNEY II UNI MED TIBIA INSERT TRIAL SZ 9-10 10MM
00885556691892JOURNEY II UNI MED TIBIA INSERT TRIAL SZ 9-10 9MM
00885556691885JOURNEY II UNI MED TIBIA INSERT TRIAL SZ 9-10 8MM
00885556691786JOURNEY II UNI MED TIBIA INSERT TRIAL SZ 7-8 14MM
00885556691779JOURNEY II UNI MED TIBIA INSERT TRIAL SZ 7-8 13MM
00885556691762JOURNEY II UNI MED TIBIA INSERT TRIAL SZ 7-8 12MM
00885556691755JOURNEY II UNI MED TIBIA INSERT TRIAL SZ 7-8 11MM
00885556691748JOURNEY II UNI MED TIBIA INSERT TRIAL SZ 7-8 10MM
00885556691731JOURNEY II UNI MED TIBIA INSERT TRIAL SZ 7-8 9MM
00885556691724JOURNEY II UNI MED TIBIA INSERT TRIAL SZ 7-8 8MM
00885556691694JOURNEY II UNI LAT TIBIA INSERT TRIAL SZ 6-7 14MM

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