HD 1200 72203404

GUDID 00885554027426

KIT SPANISH HD 1200 AUTOCLAVABLE CAMER

Smith & Nephew, Inc.

Camera control unit

• Primary Device ID: 00885554027426
• NIH Device Record Key: b0c0de30-56b1-4145-b57e-64d091461eff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HD 1200
• Version Model Number: 72203404
• Catalog Number: 72203404
• 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: true
• 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
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885554027426 [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