Total Wrist Fusion 186200ND

GUDID 00885556846599

STAINLESS STEEL LOCK SCREW FOR DIA. 2.7MM SCREW

Smith & Nephew, Inc.

Implantable bone washer

• Primary Device ID: 00885556846599
• NIH Device Record Key: 8400671d-d9a7-4e7c-9704-13c571066a12
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Total Wrist Fusion
• Version Model Number: 186200ND
• Catalog Number: 186200ND
• 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: true
• Lot Batch: true
• Serial Number: false
• 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	00885556846599 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K093163

FDA Product Code

• HRS: Plate, fixation, bone

Sterilization

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

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

[00885556846599]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-11-06
• Device Publish Date: 2023-10-27

On-Brand Devices [Total Wrist Fusion]

• 00885556819708: SCREW AND LOCK SCREW - STAINLESS STEEL DIA. 2.7MM L.18MM
• 00885556819685: SCREW AND LOCK SCREW - STAINLESS STEEL DIA. 2.7MM L.16MM
• 00885556819661: SCREW AND LOCK SCREW - STAINLESS STEEL DIA. 2.7MM L.14MM
• 00885556819623: SCREW AND LOCK SCREW - STAINLESS STEEL DIA. 2.7MM L.10MM
• 00885556819760: SCREW AND LOCK SCREW - STAINLESS STEEL DIA. 2.7MM L.24MM
• 00885556819746: SCREW AND LOCK SCREW - STAINLESS STEEL DIA. 2.7MM L.22MM
• 00885556819722: SCREW AND LOCK SCREW - STAINLESS STEEL DIA. 2.7MM L.20MM
• 00885556846599: STAINLESS STEEL LOCK SCREW FOR DIA. 2.7MM SCREW