52781-10

GUDID 00885556909362

Hip Pointer Gauge

Smith & Nephew, Inc.

Orthopaedic prosthesis implantation positioning instrument, reusable

• Primary Device ID: 00885556909362
• NIH Device Record Key: a8b3161b-7df3-4309-a0ce-4c6147cf7b1c
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 52781-10
• Catalog Number: 52781-10
• Company DUNS: 045483575
• 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: false
• Serial Number: true
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556909362 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K193307

FDA Product Code

• OLO: Orthopedic stereotaxic instrument

Sterilization

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

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

[00885556909362]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-05-16
• Device Publish Date: 2025-05-08

Devices Manufactured by Smith & Nephew, Inc.

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• 00885556919729 - Real Intelligence: 2026-03-18 Real Intelligence Tablet XT
• 00885556919743 - Real Intelligence: 2026-03-18 Real Intelligence Console Cart Column XT
• 00885556919750 - Real Intelligence: 2026-03-18 Real Intelligence Console Cart Base XT
• 00885556919767 - Real Intelligence: 2026-03-18 Real Intelligence Camera Cart Column XT
• 00885556919774 - Real Intelligence: 2026-03-18 Real Intelligence Camera Cart Base XT
• 00885556924198 - Real Intelligence: 2026-03-18 RI LITE BALL JOINT TRACKER INSTRUMENTS
• 00885556924204 - Real Intelligence: 2026-03-18 RI Universal Tracker Clamp