eudamed_udi
Primary ID: 28436542221485
GMB - Mueller HInton (UDI 28436542221485)
Manufactured by Reactivos para Diagnóstico
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GMB - Mueller HInton - Primary ID 28436542221485
Device Regulatory Overview
The GMB - Mueller HInton (Model/Catalog Number: 1123) is a medical device manufactured by Reactivos para Diagnóstico. This product is indexed under FDA Product Code / Category Classification W0104010403 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1123
- Product Code / EMDN
- W0104010403
- Device Name
- GMB - Mueller HInton Mod.
- Database Sync Date
- 2026-08-09 17:45:29
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 GMB - Mueller HInton?
The registered manufacturer of record for GMB - Mueller HInton is Reactivos para Diagnóstico.
What is the Primary UDI-DI identifier for GMB - Mueller HInton?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 28436542221485.
What classification code is assigned to this device?
This device is registered under product classification code W0104010403.
Similar Classification Devices (W0104010403)
Other Devices by Reactivos para Diagnóstico
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