VersaCross™ Large Access Trasseptal Dilator VLA0202

GUDID 00685447020295

Large Access Transseptal Dilator

Baylis Médicale Cie Inc

Vascular guide-catheter, single-use

• Primary Device ID: 00685447020295
• NIH Device Record Key: 239e086f-1bc7-4542-8013-3b69f180f935
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VersaCross™ Large Access Trasseptal Dilator
• Version Model Number: VLA0202
• Catalog Number: VLA0202
• 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: false
• 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

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00685447020295 [Primary]

FDA Product Code

• DRE: DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION

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: 2025-03-05
• Device Publish Date: 2025-02-25

On-Brand Devices [VersaCross™ Large Access Trasseptal Dilator]

• 00685447020295: Large Access Transseptal Dilator
• 00685447020288: Large Access Transseptal Dilator