GEMINI 3004

GUDID 03596010113702

LIGHT CABLE 2MM X 8FT

Smith & Nephew, Inc.

Electrical-only medical device connection cable, reusable

• Primary Device ID: 03596010113702
• NIH Device Record Key: 17ed1adc-f9bd-4b9c-b63e-32714c4e024e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GEMINI
• Version Model Number: 3004
• Catalog Number: 3004
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	03596010113702 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K914919

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

Sterilization

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

[03596010113702]

Moist Heat or Steam Sterilization

[03596010113702]

Moist Heat or Steam Sterilization

[03596010113702]

Moist Heat or Steam Sterilization

[03596010113702]

Moist Heat or Steam Sterilization

[03596010113702]

Moist Heat or Steam Sterilization

[03596010113702]

Moist Heat or Steam Sterilization

[03596010113702]

Moist Heat or Steam Sterilization

[03596010113702]

Moist Heat or Steam Sterilization

[03596010113702]

Moist Heat or Steam Sterilization

[03596010113702]

Moist Heat or Steam Sterilization

[03596010113702]

Moist Heat or Steam Sterilization

[03596010113702]

Moist Heat or Steam Sterilization

[03596010113702]

Moist Heat or Steam Sterilization

[03596010113702]

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: 2015-08-30

On-Brand Devices [GEMINI]

• 00885554008739: LT GUIDE GEMINI 4MM X 12FT
• 03596010528933: GEMINI UNIVERSAL LT GUIDE 4MM
• 03596010430847: LIGHT GUIDE 6MM 10FT
• 03596010251107: LT. GUIDE GEMINI 5MM X 12FT
• 03596010113702: LIGHT CABLE 2MM X 8FT
• 03596010113634: GEMINI LIGHT CABLE 4MM X 8 FT