gudid
Primary ID: FlowScreen CT
FlowScreen (UDI FlowScreen CT)
Manufactured by eResearchTechnology GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FlowScreen - Primary ID FlowScreen CT
Device Regulatory Overview
The FlowScreen (Model/Catalog Number: FlowScreen CT) is a medical device manufactured by eResearchTechnology GmbH. This product is indexed under FDA Product Code / Category Classification BTY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FlowScreen CT
- Product Code / EMDN
- BTY
- Device Name
- diagnostic spirometer for recording and assessing pulmonary function
- Database Sync Date
- 2026-08-09 09:26:03
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 FlowScreen?
The registered manufacturer of record for FlowScreen is eResearchTechnology GmbH.
What is the Primary UDI-DI identifier for FlowScreen?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FlowScreen CT.
What classification code is assigned to this device?
This device is registered under product classification code BTY.
Similar Classification Devices (BTY)
Other Devices by eResearchTechnology GmbH
Programmatic Export
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JSON API Endpoint