eudamed_udi
Primary ID: 38436542225114
SELENITE BROTH BASE (UDI 38436542225114)
Manufactured by Reactivos para Diagnóstico
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SELENITE BROTH BASE - Primary ID 38436542225114
Device Regulatory Overview
The SELENITE BROTH BASE (Model/Catalog Number: 02-598-005) is a medical device manufactured by Reactivos para Diagnóstico. This product is indexed under FDA Product Code / Category Classification W0104010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 02-598-005
- Product Code / EMDN
- W0104010101
- Device Name
- Selenite Broth Base-DCM
- Database Sync Date
- 2026-08-09 16:29:38
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 SELENITE BROTH BASE?
The registered manufacturer of record for SELENITE BROTH BASE is Reactivos para Diagnóstico.
What is the Primary UDI-DI identifier for SELENITE BROTH BASE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 38436542225114.
What classification code is assigned to this device?
This device is registered under product classification code W0104010101.
Similar Classification Devices (W0104010101)
Other Devices by Reactivos para Diagnóstico
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