Stop Solution 34-2325-51

GUDID 07333066000459

Stop Solution

Phadia AB

Plasma protein IVD, reagent

• Primary Device ID: 07333066000459
• NIH Device Record Key: 0d622c2e-c7f3-4846-b513-899dd1bb1fee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Stop Solution
• Version Model Number: 34-2325-51
• Catalog Number: 34-2325-51
• Company DUNS: 354019424
• Company Name: Phadia 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: false
• 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

Customer Support Contacts

• Phone: +469999999999
• Email: xx@xx.xx

Operating and Storage Conditions

• Storage Environment Temperature: Between 2 Degrees Celsius and 32 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	07333066000459 [Package]; Contains: 07333066019871; Package: [6 Units]; In Commercial Distribution
GS1	07333066019871 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K051218

FDA Product Code

• DHB: System, test, radioallergosorbent (rast) immunological

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-04-08
• Device Publish Date: 2019-03-29

On-Brand Devices [Stop Solution]

• 07333066012483: Stop Solution
• 07333066011523: Stop Solution
• 07333066000657: Stop Solution
• 07333066000459: Stop Solution