PLUS E0017042-1

GUDID 00885556789414

SL-MIA STEM INSERTER

Smith & Nephew, Inc.

Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable

• Primary Device ID: 00885556789414
• NIH Device Record Key: 26612f5e-06af-4f5b-be2c-56aa0fde85a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PLUS
• Version Model Number: E0017042-1
• Catalog Number: E0017042-1
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556789414 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K113789

FDA Product Code

• LZO: Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

Sterilization

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

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

[00885556789414]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-07-06
• Device Publish Date: 2020-06-26

On-Brand Devices [PLUS]

• 00885556696125: SL-MIA STEM INSERTER
• 00885556760697: EXTRACTION SCREW WITH LASERMARKS
• 00885556789414: SL-MIA STEM INSERTER
• 00885556784754: PLUS RASP