Primary Device ID | 00885556238691 |
NIH Device Record Key | c80099ff-cd4e-4f7e-afb7-5264f3eed35d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | JOURNEY II XR |
Version Model Number | 74014478 |
Catalog Number | 74014478 |
Company DUNS | 109903521 |
Company Name | Smith & Nephew, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00885556238691 [Primary] |
JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
[00885556238691]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-11-25 |
00885556698020 | JOURNEY II XR TIBIAL DRILL GUIDE SIZE 7-8 |
00885556698013 | JOURNEY II XR TIBIAL DRILL GUIDE SIZE 5-6 |
00885556698006 | JOURNEY II XR TIBIAL DRILL GUIDE SIZE 3-4 |
00885556697993 | JOURNEY II XR TIBIAL DRILL GUIDE SIZE 1-2 |
00885556696088 | JOURNEY II XR TIBIAL KEEL DRILL |
00885556696064 | JOURNEY II XR TIBIAL ANTERIOR KEEL PUNCH SZ 3-8 |
00885556696057 | JOURNEY II XR TIBIAL ANTERIOR KEEL PUNCH SZ 1-2 |
00885556696040 | JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 7-8 |
00885556696033 | JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 5-6 |
00885556696026 | JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 3-4 |
00885556696019 | JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 1-2 |
00885556696002 | JOURNEY II XR TIBIAL PUNCH GUIDE SIZE 8 |
00885556695999 | JOURNEY II XR TIBIAL PUNCH GUIDE SIZE 7 |
00885556695982 | JOURNEY II XR TIBIAL PUNCH GUIDE SIZE 6 |
00885556695975 | JOURNEY II XR TIBIAL PUNCH GUIDE SIZE 5 |
00885556695968 | JOURNEY II XR TIBIAL PUNCH GUIDE SIZE 4 |
00885556695951 | JOURNEY II XR TIBIAL PUNCH GUIDE SIZE 3 |
00885556695944 | JOURNEY II XR TIBIAL PUNCH GUIDE SIZE 2 |
00885556695937 | JOURNEY II XR TIBIAL PUNCH GUIDE SIZE 1 |
00885556695920 | JOURNEY II XR INSERT HOLDER CADDY |
00885556695913 | JOURNEY II XR TIBIAL FULL PUNCH TRAY |
00885556694008 | JOURNEY II XR TIBIAL PIN AND PUNCH TRAY |
00885556693995 | JOURNEY II XR MAIN INSTRUMENT TRAY |
00885556692561 | JOURNEY II XR TIB BASE COVER SZ 7-8 |
00885556692554 | JOURNEY II XR TIB BASE COVER SZ 5-6 |
00885556692547 | JOURNEY II XR TIB BASE COVER SZ 3-4 |
00885556692530 | JOURNEY II XR TIB BASE COVER SZ 1-2 |
00885556689226 | JII XR FINAL KEEL PUNCH SIZE 5-6 |
00885556689219 | JII XR FINAL KEEL PUNCH SIZE 3-4 |
00885556689141 | XR TIBIAL INSERT TRIAL SZ 1-2 LT LATERAL -2 DEG 11MM |
00885556689134 | XR TIBIAL INSERT TRIAL SZ 7-8 RT LATERAL -2 DEG 12MM |
00885556689127 | XR TIBIAL INSERT TRIAL SZ 7-8 RT LATERAL -2 DEG 11MM |
00885556689110 | XR TIBIAL INSERT TRIAL SZ 7-8 RT LATERAL -2 DEG 10MM |
00885556689103 | XR TIBIAL INSERT TRIAL SZ 7-8 RT LATERAL -2 DEG 9MM |
00885556689097 | XR TIBIAL INSERT TRIAL SZ 7-8 RT LATERAL -2 DEG 8MM |
00885556689080 | XR TIBIAL INSERT TRIAL SZ 7-8 RT MEDIAL -2 DEG 12MM |
00885556689073 | XR TIBIAL INSERT TRIAL SZ 7-8 RT MEDIAL -2 DEG 11MM |
00885556689066 | XR TIBIAL INSERT TRIAL SZ 7-8 RT MEDIAL -2 DEG 10MM |
00885556689059 | XR TIBIAL INSERT TRIAL SZ 7-8 RT MEDIAL -2 DEG 9MM |
00885556689042 | XR TIBIAL INSERT TRIAL SZ 7-8 RT MEDIAL -2 DEG 8MM |
00885556689035 | XR TIBIAL INSERT TRIAL SZ 7-8 LT LATERAL -2 DEG 12MM |
00885556689028 | XR TIBIAL INSERT TRIAL SZ 7-8 LT LATERAL -2 DEG 11MM |
00885556689011 | XR TIBIAL INSERT TRIAL SZ 7-8 LT LATERAL -2 DEG 10MM |
00885556689004 | XR TIBIAL INSERT TRIAL SZ 7-8 LT LATERAL -2 DEG 9MM |
00885556688991 | XR TIBIAL INSERT TRIAL SZ 7-8 LT LATERAL -2 DEG 8MM |
00885556688984 | XR TIBIAL INSERT TRIAL SZ 7-8 LT MEDIAL -2 DEG 12MM |
00885556688977 | XR TIBIAL INSERT TRIAL SZ 7-8 LT MEDIAL -2 DEG 11MM |
00885556688960 | XR TIBIAL INSERT TRIAL SZ 7-8 LT MEDIAL -2 DEG 10MM |
00885556688953 | XR TIBIAL INSERT TRIAL SZ 7-8 LT MEDIAL -2 DEG 9MM |
00885556688946 | XR TIBIAL INSERT TRIAL SZ 7-8 LT MEDIAL -2 DEG 8MM |