72202956S

GUDID 00885554024197

VIDEOARTHROSCOPE SD 4MM X 30 DEG

Smith & Nephew, Inc.

Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable Rigid optical arthroscope, reusable

• Primary Device ID: 00885554024197
• NIH Device Record Key: 28301586-1a56-456f-a1bf-ab89adc9c102
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 72202956S
• Catalog Number: 72202956S
• 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: false
• Serial Number: true
• 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
• 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
• 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	00885554024197 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K043395

FDA Product Code

• HRX: ARTHROSCOPE

Sterilization

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

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

[00885554024197]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-01-31
• Device Publish Date: 2015-09-28

Devices Manufactured by Smith & Nephew, Inc.

• 00885556902738 - INTELLIO SHIFT: 2024-05-15 NEO CONTROLLER REFURBISH
• 00885556630761 - Q-FIX: 2024-05-14 DISPOSABLE 1.8MM Q-FIX DRILL
• 00885556630785 - Q-FIX: 2024-05-14 REUSABLE 1.8MMQ-FIX DRILL GUIDE
• 00885556918333 - R3: 2024-05-10 FEMORAL OSTEOTOMY RULER
• 00885556817667 - TULA: 2024-05-07 TULA KIT- UNILATERAL (NST007068)
• 00885556890745 - Q-FIX: 2024-05-06 Q-FIX ULTRA
• 00885556890752 - ULTRABRACE: 2024-05-06 ULTRABRACE KIT
• 00885556890769 - FOOTPRINT: 2024-05-06 FOOTPRINT MINI PK 3.5MM