L10 0220220300

GUDID 07613327051377

LED Light Source with AIM Technology

STRYKER CORPORATION

Endoscopic light source, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered

• Primary Device ID: 07613327051377
• NIH Device Record Key: a859487f-02c1-415e-b6c3-205c0f320af5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: L10
• Version Model Number: 0220220300
• Catalog Number: 0220220300
• Company DUNS: 187502109
• Company Name: STRYKER CORPORATION
• 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(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327051377 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142310

FDA Product Code

• OWN: Confocal optical imaging

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: 2019-02-21
• Device Publish Date: 2016-09-23

Devices Manufactured by STRYKER CORPORATION

• 07613327141870 - SOLIS: 2024-06-28 SPECIALTY INSERTER WITH STOP
• 07613327141924 - SOLIS: 2024-06-28 SPECIALTY AS INSERTER WITH STOP
• 07613327261707 - OPUS: 2024-06-28 NUT WRENCH
• 07613327261714 - OPUS: 2024-06-28 SCREWDRIVER
• 07613327261721 - OPUS: 2024-06-28 ANTI-ROTATION WRENCH
• 07613327265132 - XIA PRECISION SYSTEM: 2024-06-28 XIA CANNULATED ROUND HANDLE RATCHET
• 07613327265170 - XIA PRECISION SYSTEM: 2024-06-28 XIA CANNULATED T-HANDLE NON-RATCHET
• 07613327265217 - XIA PRECISION SYSTEM: 2024-06-28 XIA CANNULATED ROUND HANDLE NON-RATCHET