500XL 72200598

GUDID 00885554012842

KIT ENGLISH 500XL

Smith & Nephew, Inc.

Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 00885554012842
• NIH Device Record Key: c0f41424-9230-42d4-80da-3a749abe08c6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 500XL
• Version Model Number: 72200598
• Catalog Number: 72200598
• 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	00885554012842 [Primary]

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

On-Brand Devices [500XL]

• 00885556586297: RFB LIGHT SCE 500XL XENON
• 00885556586280: SVCE REPL LIGHT SCE 500XL XENON
• 00885556571392: RFB LIGHT SOURCE 500XL XENON
• 00885556541067: KIT KOREAN 500XL
• 00885554015997: KIT PORTUGUESE 500XL
• 00885554013122: KIT SPANISH 500XL
• 00885554012842: KIT ENGLISH 500XL
• 03596010643070: LIGHT SOURCE 500XL XENON
• 03596010643063: REPLACEMENT. LAMP MODULE 500XL XENON