HD 1200 72203361

GUDID 03596010657503

CAMERA CONTROL UNIT HD 1200 AUTOCLAVAB

Smith & Nephew, Inc.

Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit Camera control unit

• Primary Device ID: 03596010657503
• NIH Device Record Key: cc116ac4-be98-4142-950d-61c9d5143fdc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HD 1200
• Version Model Number: 72203361
• Catalog Number: 72203361
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	03596010657503 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K014158

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: 4
• Public Version Date: 2020-01-31
• Device Publish Date: 2015-08-29

On-Brand Devices [HD 1200]

• 00885554027518: KIT CHINESE HD 1200 AUTOCLAVABLE CAMER
• 00885554027501: KIT KOREAN HD 1200 AUTOCLAVABLE CAMERA
• 00885554027464: KIT PORTUGUESE HD 1200 AUTOCLAVABLE CA
• 00885554027426: KIT SPANISH HD 1200 AUTOCLAVABLE CAMER
• 00885554027402: KIT UK HD 1200 AUTOCLAVABLE CAMERA
• 00885554025897: SVCE REPL CAMERA HEAD HD 1200 AC
• 00885554025880: SVCE REPL CAMERA CONTROL UNIT HD1200
• 00885554024920: KIT HD 1200 AUTOCLAVABLE CAMERA SYST
• 03596010657503: CAMERA CONTROL UNIT HD 1200 AUTOCLAVAB
• 03596010657497: CAMERA HEAD HD 1200 AUTOCLAVABLE