Anti-Human IgG Conjugate 404558

GUDID 10888234500469

For Use with Pak2-LE

IMMUCOR GTI DIAGNOSTICS, INC.

Human platelet antigen (HPA) multiple antibody screening/identification IVD, reagent

• Primary Device ID: 10888234500469
• NIH Device Record Key: 594ffd14-fc92-41b1-a562-cbc1cddd4d19
• Commercial Distribution Discontinuation: 2017-12-15
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Anti-Human IgG Conjugate
• Version Model Number: 404558
• Catalog Number: 404558
• Company DUNS: 606034197
• Company Name: IMMUCOR GTI DIAGNOSTICS, INC.
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 855-466-8267
• Email: waukeshatechsupport@immucor.co

Operating and Storage Conditions

• Storage Environment Temperature: Between 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	10888234500469 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• BK930032

FDA Product Code

• MYP: Test,Platelet Antibody

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-08-01
• Device Publish Date: 2016-07-08

On-Brand Devices [Anti-Human IgG Conjugate]

• 10888234500469: For Use with Pak2-LE
• 10888234500452: For Use with Pak12G
• 10888234500384: For Use with PF4 IgG (HAT13G & HAT45G)