Follicle Aspiration Set Reduced Single Lumen, Luer

GUDID 17350025915484

Vitrolife Sweden AB

IVF oocyte aspiration needle, single-use

• Primary Device ID: 17350025915484
• NIH Device Record Key: 7957320a-7192-4ad8-9101-f95774999ce1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Follicle Aspiration Set Reduced Single Lumen, Luer
• Version Model Number: 17180
• Company DUNS: 631805488
• Company Name: Vitrolife Sweden AB
• 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: true
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	07350025915487 [Primary]
GS1	17350025915484 [Package]; Contains: 07350025915487; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• MQE: Needle, Assisted Reproduction

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: 2024-12-04
• Device Publish Date: 2024-11-26

On-Brand Devices [Follicle Aspiration Set Reduced Single Lumen, Luer]

• 17350025915484: 17180
• 17350025915477: 17179