7210498

GUDID 00885556539682

MTOLAPAROSCOPE 5.5 X O DEG X 170 WL

Smith & Nephew, Inc.

Rigid optical laparoscope

• Primary Device ID: 00885556539682
• NIH Device Record Key: 4ac790e5-c035-472e-9ea5-ef9cb0117bcd
• Commercial Distribution Discontinuation: 2017-04-03
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 7210498
• Catalog Number: 7210498
• 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)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	00885556539682 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K980604

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

Sterilization

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

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

Moist Heat or Steam Sterilization

[00885556539682]

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: 2015-08-30

Devices Manufactured by Smith & Nephew, Inc.

• 00885556903421 - EVOS: 2025-09-10 EVOS PELVIC 5.0MM X 135MM CANNULATED SCREW FULLY THREADED
• 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