Follicle Aspiration Set Double Lumen

GUDID 17350025915064

Vitrolife Sweden AB

IVF oocyte aspiration needle, single-use

• Primary Device ID: 17350025915064
• NIH Device Record Key: e6e12e34-2434-438e-b0f8-e698632f0346
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Follicle Aspiration Set Double Lumen
• Version Model Number: 17102
• 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: 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 Identifiers

Device Issuing Agency	Device ID
GS1	07350025915067 [Primary]
GS1	17350025915064 [Package]; Contains: 07350025915067; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K161970

FDA Product Code

• MQE: Needle, Assisted Reproduction

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-09-26

On-Brand Devices [ Follicle Aspiration Set Double Lumen]

• 17350025915415: 17168
• 17350025915408: 17161
• 17350025915392: 17158
• 17350025915347: 17151
• 17350025915330: 17150
• 17350025915323: 17148
• 17350025915255: 17131
• 17350025915231: 17129
• 17350025915163: 17114
• 17350025915132: 17111
• 17350025915125: 17109
• 17350025915118: 17108
• 17350025915095: 17105
• 17350025915064: 17102