VersaCross RF Wire

GUDID 00685447003281

1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)

Baylis Médicale Cie Inc

Endoscopic electrosurgical electrode, monopolar, single-use

• Primary Device ID: 00685447003281
• NIH Device Record Key: 08b36318-6db2-4461-a849-08dbbed83e6d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VersaCross RF Wire
• Version Model Number: VXW-35-180-J
• Company DUNS: 249225954
• Company Name: Baylis Médicale Cie 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com
• Phone: 5144889801
• Email: info@baylismedical.com

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00685447003281 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150709

FDA Product Code

• DXF: Catheter, Septostomy

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-05-09
• Device Publish Date: 2019-05-01

On-Brand Devices [VersaCross RF Wire]

• 00685447003311: 1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)
• 00685447003304: 1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)
• 00685447003298: 1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)
• 00685447003281: 1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)
• 00685447011200: 1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)
• 00685447011194: 1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)
• 00685447011187: 1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)
• 00685447011170: 1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)
• 00685447011118: 1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)
• 00685447011101: 1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)
• 00685447011095: 1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)
• 00685447011088: 1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)
• 00685447018872: 1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)
• 00685447018865: 1 x VersaCross RF Wire; 1 x Connector Cable (Single Use)