Connected OR Hub 0240-200-200

GUDID 07613327601695

STRYKER CORPORATION

Operating room audiovisual data/device management system

• Primary Device ID: 07613327601695
• NIH Device Record Key: 1d16cf25-be6d-48f3-afa3-a102a35625cb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Connected OR Hub
• Version Model Number: 0240200200
• Catalog Number: 0240-200-200
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327601695 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K241401

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-12
• Device Publish Date: 2025-06-04

On-Brand Devices [Connected OR Hub]

• 07613327419153: 0240200103
• 07613327419146: 0240200102
• 07613327512243: 0240200101
• 07613327413281: Device Management Control System
• 07613327601695: 0240200200