Negative Control Serum 628209

GUDID 10888234400592

For Use with LIFECODES Class I ID

IMMUCOR GTI DIAGNOSTICS, INC.

HLA class I antigen tissue typing IVD, kit, multiplex

• Primary Device ID: 10888234400592
• NIH Device Record Key: 58b5c2bc-865b-49fd-954e-baf01e2530f0
• Commercial Distribution Discontinuation: 2018-12-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Negative Control Serum
• Version Model Number: 628209
• Catalog Number: 628209
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

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

Operating and Storage Conditions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10888234400592 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• BK040035

FDA Product Code

• MZI: Test,Qualitative,For Hla,Non-Diagnostic

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: 2019-01-10
• Device Publish Date: 2016-09-15

On-Brand Devices [Negative Control Serum]

• 10888234400622: For Use with LIFECODES Class II IDv2
• 10888234400592: For Use with LIFECODES Class I ID
• 10888234400547: For Use with LIFECODES LifeScreen Deluxe