SelectaLyte (Chloride Electrode) (UDI 3910)
Manufactured by AWARENESS TECHNOLOGY, INCORPORATED
Device Regulatory Overview
The SelectaLyte (Chloride Electrode) (Model/Catalog Number: 3910) is a medical device manufactured by AWARENESS TECHNOLOGY, INCORPORATED. This product is indexed under FDA Product Code / Category Classification CGZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3910
- Product Code / EMDN
- CGZ
- Device Name
- Database Sync Date
- 2026-08-09 09:49:40
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of SelectaLyte (Chloride Electrode)?
The registered manufacturer of record for SelectaLyte (Chloride Electrode) is AWARENESS TECHNOLOGY, INCORPORATED.
What is the Primary UDI-DI identifier for SelectaLyte (Chloride Electrode)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3910.
What classification code is assigned to this device?
This device is registered under product classification code CGZ.
Similar Classification Devices (CGZ)
Other Devices by AWARENESS TECHNOLOGY, INCORPORATED
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