ENDO - KNEE E0016307-7

GUDID 00885556738351

RIGHT 8.5MM FEMORAL OFFSET AIMER

Smith & Nephew, Inc.

Orthopaedic implant aiming arm

• Primary Device ID: 00885556738351
• NIH Device Record Key: c9f478e0-0957-4d2f-901e-8f30112a6cfd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ENDO - KNEE
• Version Model Number: E0016307-7
• Catalog Number: E0016307-7
• Company DUNS: 109903521
• Company Name: Smith & Nephew, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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

Customer Support Contacts

• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556738351 [Primary]

FDA Product Code

• NBH: Accessories, arthroscopic

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

[00885556738351]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-03-04
• Device Publish Date: 2019-02-01

On-Brand Devices [ENDO - KNEE]

• 00885556738375: RIGHT 9.5MM FEMORAL OFFSET AIMER
• 00885556738351: RIGHT 8.5MM FEMORAL OFFSET AIMER
• 00885556738337: RIGHT 7.5MM FEMORAL OFFSET AIMER
• 00885556738313: RIGHT 6.5MM FEMORAL OFFSET AIMER
• 00885556738283: LEFT 9.5MM FEMORAL OFFSET AIMER
• 00885556738252: LEFT 8.5MM FEMORAL OFFSET AIMER
• 00885556738238: LEFT 7.5MM FEMORAL OFFSET AIMER
• 00885556738207: LEFT 6.5MM FEMORAL OFFSET AIMER