LENS Antenna 72204938

GUDID 00885556651421

LENS CCU WI-FI ANTENNA

Smith & Nephew, Inc.

Endoscopic video imaging system

• Primary Device ID: 00885556651421
• NIH Device Record Key: f7fb7581-1c0b-4c38-b515-b6e0870f0247
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LENS Antenna
• Version Model Number: 72204938
• Catalog Number: 72204938
• 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: 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
• 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	00885556651421 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153606

FDA Product Code

• GCJ: Laparoscope, General & Plastic Surgery

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-06-13

Devices Manufactured by Smith & Nephew, Inc.

• 00885556903438 - EVOS: 2025-09-08 EVOS PELVIC 5.0MM X 140MM CANNULATED SCREW FULLY THREADED
• 00885556903445 - EVOS: 2025-09-08 EVOS PELVIC 5.0MM X 145MM CANNULATED SCREW FULLY THREADED
• 00885556903452 - EVOS: 2025-09-08 EVOS PELVIC 5.0MM X 150MM CANNULATED SCREW FULLY THREADED
• 00885556903469 - EVOS: 2025-09-08 EVOS PELVIC 5.0MM X 50MM CANNULATED SCREW PARTIALLY THREADED 32MM
• 00885556903476 - EVOS: 2025-09-08 EVOS PELVIC 5.0MM X 55MM CANNULATED SCREW PARTIALLY THREADED 32MM
• 00885556903483 - EVOS: 2025-09-08 EVOS PELVIC 5.0MM X 60MM CANNULATED SCREW PARTIALLY THREADED 32MM
• 00885556903490 - EVOS: 2025-09-08 EVOS PELVIC 5.0MM X 65MM CANNULATED SCREW PARTIALLY THREADED 32MM
• 00885556903506 - EVOS: 2025-09-08 EVOS PELVIC 5.0MM X 70MM CANNULATED SCREW PARTIALLY THREADED 32MM