SLR-PLUS 75017273

GUDID 07611996095623

SLR-PLUS TRIAL BROACH 5

Smith & Nephew, Inc.

Femoral stem prosthesis trial

• Primary Device ID: 07611996095623
• NIH Device Record Key: deb064e3-fdcc-4a22-9448-2165bc5fdac9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SLR-PLUS
• Version Model Number: 75017273
• Catalog Number: 75017273
• 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

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
• 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
• 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	07611996095623 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123598

FDA Product Code

• KWY: Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented

Sterilization

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

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

[07611996095623]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-02-07
• Device Publish Date: 2016-08-19

On-Brand Devices [SLR-PLUS]

• 07611996095685: SLR-PLUS TRIAL BROACH 11
• 07611996095678: SLR-PLUS TRIAL BROACH 10
• 07611996095661: SLR-PLUS TRIAL BROACH 9
• 07611996095654: SLR-PLUS TRIAL BROACH 8
• 07611996095647: SLR-PLUS TRIAL BROACH 7
• 07611996095630: SLR-PLUS TRIAL BROACH 6
• 07611996095623: SLR-PLUS TRIAL BROACH 5
• 07611996095616: SLR-PLUS TRIAL BROACH 4
• 07611996095609: SLR-PLUS TRIAL BROACH 3
• 07611996095593: SLR-PLUS TRIAL BROACH 2
• 07611996095586: SLR-PLUS TRIAL BROACH 1