Vacuum Pump Tubing

GUDID 17350025914470

Vitrolife Sweden AB

Suction system catheter, general-purpose

• Primary Device ID: 17350025914470
• NIH Device Record Key: 01df9033-c083-4f8d-b70d-ad2617e355e0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vacuum Pump Tubing
• Version Model Number: 14212
• Company DUNS: 631805488
• Company Name: Vitrolife Sweden AB
• Device Count: 10
• 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	07350025914473 [Unit of Use]
GS1	17350025914470 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K991273

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: 2016-09-14

On-Brand Devices [Vacuum Pump Tubing ]

• 17350025914470: 14212
• 17350025914326: 14211
• 17350025911684: 14205
• 17350025915668: 17203
• 17350025915651: 17202
• 17350025915644: 17201