AtriClip FLEX•V A001019-4

GUDID 10840143901300

AtriClip FLEX•V device 45

ATRICURE, INC.

Ligation clip, metallic

• Primary Device ID: 10840143901300
• NIH Device Record Key: b5694ca5-b5fe-44f5-a9b1-0a26d3546dc2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AtriClip FLEX•V
• Version Model Number: ACHV45
• Catalog Number: A001019-4
• Company DUNS: 006133784
• Company Name: ATRICURE, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Length: 45 Millimeter

Operating and Storage Conditions

• Handling Environment Temperature: Between 20 Degrees Celsius and 0 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	10840143901300 [Primary]

FDA Product Code

• FZP: Clip, Implantable

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: 2023-01-13
• Device Publish Date: 2023-01-05

On-Brand Devices [AtriClip FLEX•V]

• 00818354016185: AtriClip FLEX•V device 50
• 00818354016178: AtriClip FLEX•V device 45
• 00818354016161: AtriClip FLEX•V device 40
• 00818354016154: AtriClip FLEX•V device 35
• 30840143900161: AtriClip FLEX•V device 50
• 30840143900154: AtriClip FLEX•V device 45
• 30840143900147: AtriClip FLEX•V device 40
• 30840143900130: AtriClip FLEX•V device 35
• 10840143901324: AtriClip FLEX•V device 50
• 10840143901300: AtriClip FLEX•V device 45
• 10840143901287: AtriClip FLEX•V device 40
• 10840143901263: AtriClip FLEX•V device 35