VisionPro, SYNK 0240-031-000

GUDID 07613327056068

26 Inch Wireless LED Display

STRYKER CORPORATION

Image display monitor, colour

• Primary Device ID: 07613327056068
• NIH Device Record Key: 88fcf46e-2672-40bb-9e53-477979bc2630
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VisionPro, SYNK
• Version Model Number: 0240031000
• Catalog Number: 0240-031-000
• 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
• 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	07613327056068 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K081995

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: 2018-07-06
• Device Publish Date: 2016-09-23

Devices Manufactured by STRYKER CORPORATION

• 07613327643800 - NA: 2025-12-29 WIRE COLLET
• 07613327643817 - AO: 2025-12-29 SMALL DRILL
• 07613327643824 - NA: 2025-12-29 ADJUSTABLE PIN COLLET
• 07613327643831 - NA: 2025-12-29 1/4" DRILL WITH KEY
• 07613327643848 - NA: 2025-12-29 PIN COLLET
• 07613327643855 - NA: 2025-12-29 5/32" DRILL W/KEY
• 07613327272246 - ARIA: 2025-09-25 IMPLANT IMPACTOR
• 37613327405317 - SurgiCount Safety-Sponge: 2025-09-16 Laparotomy Sponge