StatFax

GUDID 00850229007089

Digital Dry Bath

AWARENESS TECHNOLOGY, INCORPORATED

Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker Laboratory shaker

• Primary Device ID: 00850229007089
• NIH Device Record Key: 2701b4d5-447b-409a-904d-56490c5f1680
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: StatFax
• Version Model Number: 2200
• Company DUNS: 071065130
• Company Name: AWARENESS TECHNOLOGY, INCORPORATED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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	00850229007089 [Primary]

FDA Product Code

• JTQ: Bath, Incubators/Water, All

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-13
• Device Publish Date: 2023-06-05

On-Brand Devices [StatFax ]

• 00850229007102: 1904+
• 00850229007089: Digital Dry Bath
• 00850229007072: Digital Dry Bath
• 00850229007041: 3300
• 00850229007034: 4200
• 00850229007027: 4500
• 00850229007010: 4700