71931680

GUDID 00885556055892

MIS METAL OVAL PATELLA PROTECTOR 41MM

Smith & Nephew, Inc.

Surgical instrument guard, reusable

• Primary Device ID: 00885556055892
• NIH Device Record Key: 31b3c80f-3ca8-4f37-bddc-c72b9cb72a1e
• Commercial Distribution Discontinuation: 2016-07-03
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 71931680
• Catalog Number: 71931680
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556055892 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121393

FDA Product Code

• HRY: PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER

Sterilization

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

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

Moist Heat or Steam Sterilization

[00885556055892]

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: 2015-09-28

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• 00885556898925 - INTERTAN MAX: 2025-11-21 INTERTAN MAX LAG/COMP SCREW KIT - DYNAMIC - 95MM/90MM
• 00885556898932 - INTERTAN MAX: 2025-11-21 INTERTAN MAX LAG/COMP SCREW KIT - DYNAMIC - 100MM/95MM
• 00885556898949 - INTERTAN MAX: 2025-11-21 INTERTAN MAX LAG/COMP SCREW KIT - DYNAMIC - 105MM/100MM