eudamed_udi
Primary ID: 05032384005970
SXT25 SULPHAMET / TRIMETHOP (UDI 05032384005970)
Manufactured by Oxoid Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SXT25 SULPHAMET / TRIMETHOP - Primary ID 05032384005970
Device Regulatory Overview
The SXT25 SULPHAMET / TRIMETHOP (Model/Catalog Number: CT0052B) is a medical device manufactured by Oxoid Ltd. This product is indexed under FDA Product Code / Category Classification W0104080502 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CT0052B
- Product Code / EMDN
- W0104080502
- Device Name
- SULPHAMET / TRIMETHOP
- Database Sync Date
- 2026-08-09 16:48:40
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 SXT25 SULPHAMET / TRIMETHOP?
The registered manufacturer of record for SXT25 SULPHAMET / TRIMETHOP is Oxoid Ltd.
What is the Primary UDI-DI identifier for SXT25 SULPHAMET / TRIMETHOP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05032384005970.
What classification code is assigned to this device?
This device is registered under product classification code W0104080502.
Similar Classification Devices (W0104080502)
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