First Choice DRUJ and MUH TRL600MED

GUDID 00885556826621

MUH TRIAL COLLAR MEDIUM

Smith & Nephew, Inc.

Surgical implant template, reusable

• Primary Device ID: 00885556826621
• NIH Device Record Key: 9847fe32-5e72-42c1-acd5-ca7a6a874ad1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: First Choice DRUJ and MUH
• Version Model Number: TRL-600-MED
• Catalog Number: TRL600MED
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556826621 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112481

FDA Product Code

• KXE: Prosthesis, wrist, hemi-, ulnar

Sterilization

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

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

[00885556826621]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-26
• Device Publish Date: 2023-06-16

Devices Manufactured by Smith & Nephew, Inc.

• 00885556747353 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 1 LEFT
• 00885556747360 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 2 LEFT
• 00885556747377 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 3 LEFT
• 00885556747384 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 5 LEFT
• 00885556747407 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 1 RIGHT
• 00885556747414 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 2 RIGHT
• 00885556747421 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 3 RIGHT
• 00885556747438 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 4 RIGHT