DIRECT VIEW AND VIDEO SCOPES 72205880

GUDID 00885556915875

4KO VIDIOARTHROSCOPE AC 4 X 30 DEG X 160MM REVERSE POST

Smith & Nephew, Inc.

Rigid optical arthroscope, reusable

• Primary Device ID: 00885556915875
• NIH Device Record Key: 978cfaf9-9f9f-4a4f-b85b-da8379594de9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DIRECT VIEW AND VIDEO SCOPES
• Version Model Number: 72205880
• Catalog Number: 72205880
• 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: 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)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	00885556915875 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K201349

FDA Product Code

• HRX: Arthroscope

Sterilization

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

[00885556915875]

Moist Heat or Steam Sterilization

[00885556915875]

Moist Heat or Steam Sterilization

[00885556915875]

Moist Heat or Steam Sterilization

[00885556915875]

Moist Heat or Steam Sterilization

[00885556915875]

Moist Heat or Steam Sterilization

[00885556915875]

Moist Heat or Steam Sterilization

[00885556915875]

Moist Heat or Steam Sterilization

[00885556915875]

Moist Heat or Steam Sterilization

[00885556915875]

Moist Heat or Steam Sterilization

[00885556915875]

Moist Heat or Steam Sterilization

[00885556915875]

Moist Heat or Steam Sterilization

[00885556915875]

Moist Heat or Steam Sterilization

[00885556915875]

Moist Heat or Steam Sterilization

[00885556915875]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-07-01
• Device Publish Date: 2025-06-23

On-Brand Devices [DIRECT VIEW AND VIDEO SCOPES]

• 00885556915899: SERVICE REPLACEMENT 4KO VAS AC 4X 30 DEG X 160MM REVERSE POST
• 00885556915875: 4KO VIDIOARTHROSCOPE AC 4 X 30 DEG X 160MM REVERSE POST