Vacuum Pump Tubing

GUDID 17350025915651

Vitrolife Sweden AB

Vacuum tubing, single-use Disposable vacuum tubing Disposable vacuum tubing Disposable vacuum tubing Disposable vacuum tubing Disposable vacuum tubing Disposable vacuum tubing Disposable vacuum tubing Disposable vacuum tubing

• Primary Device ID: 17350025915651
• NIH Device Record Key: 2ed6b340-e664-4f48-b514-a66833df2920
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vacuum Pump Tubing
• Version Model Number: 17202
• Company DUNS: 631805488
• Company Name: Vitrolife Sweden AB
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	07350025915654 [Primary]
GS1	17350025915651 [Package]; Contains: 07350025915654; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• GAZ: Tubing, Noninvasive

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: 2019-06-20
• Device Publish Date: 2019-06-12

On-Brand Devices [Vacuum Pump Tubing]

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