Achieve CAS 74471987

GUDID 00885556074930

ACHIEVECAS COMPLETE SINGLE STAND KIT

Smith & Nephew, Inc.

Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system Orthopaedic stereotactic surgery system

• Primary Device ID: 00885556074930
• NIH Device Record Key: 7368d23f-7bdd-4fe9-a6da-4e94c4987385
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Achieve CAS
• Version Model Number: 74471987
• Catalog Number: 74471987
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556074930 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K012938

FDA Product Code

• HAW: Neurological stereotaxic Instrument

Sterilization

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

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

[00885556074930]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-11-25

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• 00885556917978 - Legion: 2024-04-10 EM PROXIMAL GUIDE - L