012710

GUDID 03596010080899

CURETTE CLOSED 5MM

Smith & Nephew, Inc.

Bone curette, reusable

• Primary Device ID: 03596010080899
• NIH Device Record Key: ea66617e-3477-4de9-a16a-6aaabfcd2c57
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 012710
• Catalog Number: 012710
• 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: true
• 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)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	03596010080899 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K940985

FDA Product Code

• HRX: ARTHROSCOPE

Sterilization

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

[03596010080899]

Moist Heat or Steam Sterilization

[03596010080899]

Moist Heat or Steam Sterilization

[03596010080899]

Moist Heat or Steam Sterilization

[03596010080899]

Moist Heat or Steam Sterilization

[03596010080899]

Moist Heat or Steam Sterilization

[03596010080899]

Moist Heat or Steam Sterilization

[03596010080899]

Moist Heat or Steam Sterilization

[03596010080899]

Moist Heat or Steam Sterilization

[03596010080899]

Moist Heat or Steam Sterilization

[03596010080899]

Moist Heat or Steam Sterilization

[03596010080899]

Moist Heat or Steam Sterilization

[03596010080899]

Moist Heat or Steam Sterilization

[03596010080899]

Moist Heat or Steam Sterilization

[03596010080899]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-01-31
• Device Publish Date: 2015-08-30

Devices Manufactured by Smith & Nephew, Inc.

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• 00885556892510 - TRIGEN MAX: 2025-05-16 TRIGEN MAX TIBIA NAIL 8MM X 26CM LEFT
• 00885556892527 - TRIGEN MAX: 2025-05-16 TRIGEN MAX TIBIA NAIL 8MM X 27CM LEFT
• 00885556892534 - TRIGEN MAX: 2025-05-16 TRIGEN MAX TIBIA NAIL 8MM X 28CM LEFT
• 00885556892541 - TRIGEN MAX: 2025-05-16 TRIGEN MAX TIBIA NAIL 8MM X 29CM LEFT
• 00885556892558 - TRIGEN MAX: 2025-05-16 TRIGEN MAX TIBIA NAIL 8MM X 30CM LEFT
• 00885556892565 - TRIGEN MAX: 2025-05-16 TRIGEN MAX TIBIA NAIL 8MM X 31CM LEFT