MedRx

GUDID 00810044580075

MEDRX, INC.

Audiometric/hearing aid tester

• Primary Device ID: 00810044580075
• NIH Device Record Key: d5bd3ece-dcc7-408b-ad30-957c76c39fde
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MedRx
• Version Model Number: Avant REMsp
• Company DUNS: 849311261
• Company Name: MEDRX, INC.
• 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: true
• 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	00810044580075 [Primary]

FDA Product Code

• ETW: Calibrator, Hearing Aid / Earphone And Analysis Systems

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: 2020-01-31
• Device Publish Date: 2016-09-24

On-Brand Devices [MedRx]

• 00810044580112: Avant AIR+
• 00810044580082: Tinnometer
• 00810044580075: Avant REMsp
• 00810044580044: Avant Stealth Audiometer
• 00810044580037: Avant REM Speech+
• 00810044580020: Avant HIT+
• 00810044580013: Avant ARC
• 00810044580006: Avant A2D+
• 00810044582963: MedRx Kiosk
• 00810044583045: MedRx AWRC
• 00810044583182: MedRx WREM