Trauma-Internal Fix E0017435-1

GUDID 00885556812754

PARALLEL WIRE AND SCREW DISTRACTOR

Smith & Nephew, Inc.

ENT elevator

• Primary Device ID: 00885556812754
• NIH Device Record Key: daded029-fb1d-428b-8007-a14f7977dc3f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trauma-Internal Fix
• Version Model Number: E0017435-1
• Catalog Number: E0017435-1
• Company DUNS: 109903521
• Company Name: Smith & Nephew, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556812754 [Primary]

FDA Product Code

• FZX: Guide, surgical, instrument

Sterilization

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

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

[00885556812754]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-07-28
• Device Publish Date: 2021-07-20

On-Brand Devices [Trauma-Internal Fix]

• 00885556794487: T25 SCREWDRIVER ONE PIECE
• 00885556794470: 3.5MM HEX HEAD SCREWDRIVER ONE PIECE
• 00885556812754: PARALLEL WIRE AND SCREW DISTRACTOR