WIESLAB ANCA Screen kit CP111

GUDID 07340058410639

Euro-Diagnostica AB

Multiple vasculitis-associated antibody IVD, kit, enzyme immunoassay (EIA)

• Primary Device ID: 07340058410639
• NIH Device Record Key: 89deb3f2-217b-405f-a63b-aeb959810fcb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WIESLAB ANCA Screen kit
• Version Model Number: CP111
• Catalog Number: CP111
• Company DUNS: 559894501
• Company Name: Euro-Diagnostica 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: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07340058410639 [Primary]

FDA Product Code

• MOB: Test System, Antineutrophil Cytoplasmic Antibodies (Anca)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-12

Devices Manufactured by Euro-Diagnostica AB

• 07340058410004 - DIASTAT anti-Ro (SS-A): 2018-07-06
• 07340058410011 - DIASTAT anti-La (SS-B): 2018-07-06
• 07340058410035 - DIASTAT anti-dsDNA: 2018-07-06
• 07340058410059 - DIASTST anti-Sm: 2018-07-06
• 07340058410110 - DIASTAT anti-thyroglobulin: 2018-07-06
• 07340058410134 - DIASTAT anti-Thyroid Peroxidase: 2018-07-06
• 07340058410417 - DIASTAT anti-Mitochondrial: 2018-07-06
• 07340058410431 - CCPoint: 2018-07-06