gudid
Primary ID: 304.333.000
CITREX H3 (UDI 304.333.000)
Manufactured by IMT Analytics AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CITREX H3 - Primary ID 304.333.000
Device Regulatory Overview
The CITREX H3 (Model/Catalog Number: 304.333.000) is a medical device manufactured by IMT Analytics AG. This product is indexed under FDA Product Code / Category Classification BXY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 304.333.000
- Product Code / EMDN
- BXY
- Device Name
- Flowmeter, calibration, gas
- Database Sync Date
- 2026-08-09 09:16:07
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 CITREX H3?
The registered manufacturer of record for CITREX H3 is IMT Analytics AG.
What is the Primary UDI-DI identifier for CITREX H3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 304.333.000.
What classification code is assigned to this device?
This device is registered under product classification code BXY.
Similar Classification Devices (BXY)
Other Devices by IMT Analytics AG
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