Panoscreen I, II, and III 0002381

GUDID 10888234000303

Panoscreen I, II, and III is intended for use in the detection of unexpected IgG antibodies to red blood cells by manual tube method. The configuratio

IMMUCOR, INC.

Antibody screening reagent red blood cell IVD, kit, agglutination

• Primary Device ID: 10888234000303
• NIH Device Record Key: 9784b8e1-a18b-45a6-b033-8002479699eb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Panoscreen I, II, and III
• Version Model Number: 0002381
• Catalog Number: 0002381
• Company DUNS: 061446282
• Company Name: IMMUCOR, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Device Kit: true
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1-855-466-8267
• Email: tech_support@immucor.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 1 Degrees Celsius and 10 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	10888234000303 [Primary]

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: 2014-09-24

On-Brand Devices [Panoscreen I, II, and III]

• 10888234000303: Panoscreen I, II, and III is intended for use in the detection of unexpected IgG antibodies to r
• 10888234000280: Panoscreen I, II, and III is intended for use in the detection of unexpected IgG antibodies to r