Connected OR HUB 0240200101

GUDID 07613327512243

STRYKER CORPORATION

Endoscopic device remote control Endoscopic device remote control Endoscopic device remote control Endoscopic device remote control Endoscopic device remote control Endoscopic device remote control Endoscopic device remote control Endoscopic device remote control Endoscopic device remote control Endoscopic device remote control Endoscopic device remote control Endoscopic device remote control Endoscopic device remote control Endoscopic device remote control Endoscopic device remote control

• Primary Device ID: 07613327512243
• NIH Device Record Key: 70e2db18-2333-48ec-99bc-00015b3e513e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Connected OR HUB
• Version Model Number: 0240200101
• Catalog Number: 0240200101
• 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: 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(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	07613327512243 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K201434

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: 2021-06-03
• Device Publish Date: 2021-05-26

On-Brand Devices [Connected OR HUB]

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