Redi-Check Photometer QC E305

GUDID 00850229007119

Photometer Quality Control

AWARENESS TECHNOLOGY, INCORPORATED

Optical instrument calibration/verification solution IVD Optical instrument performance standard calibrator/control IVD, single-use

• Primary Device ID: 00850229007119
• NIH Device Record Key: dafabe22-5081-4406-95ab-43aff4874190
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Redi-Check Photometer QC
• Version Model Number: Redi-Check Photometer QC
• Catalog Number: E305
• Company DUNS: 071065130
• Company Name: AWARENESS TECHNOLOGY, INCORPORATED
• 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: true
• 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	00850229007119 [Primary]

FDA Product Code

• JFS: Coulometric, Chloride

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-11-08
• Device Publish Date: 2016-06-30

Devices Manufactured by AWARENESS TECHNOLOGY, INCORPORATED

• 00850229007010 - StatFax: 2023-06-13
• 00850229007027 - StatFax: 2023-06-13
• 00850229007034 - StatFax: 2023-06-13
• 00850229007041 - StatFax: 2023-06-13
• 00850229007072 - StatFax: 2023-06-13 Digital Dry Bath
• 00850229007089 - StatFax: 2023-06-13 Digital Dry Bath
• 00850229007102 - StatFax: 2023-06-13
• 00850229007126 - LumiStat: 2023-06-13