eudamed_udi
Primary ID: 08435295164694
DESOXYCHOLATE AGAR (UDI 08435295164694)
Manufactured by Laboratorios Conda S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DESOXYCHOLATE AGAR - Primary ID 08435295164694
Device Regulatory Overview
The DESOXYCHOLATE AGAR (Model/Catalog Number: 1020) is a medical device manufactured by Laboratorios Conda S.A.. This product is indexed under FDA Product Code / Category Classification W0104010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1020
- Product Code / EMDN
- W0104010101
- Device Name
- DESOXYCHOLATE AGAR
- Database Sync Date
- 2026-08-09 16:29:04
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 DESOXYCHOLATE AGAR?
The registered manufacturer of record for DESOXYCHOLATE AGAR is Laboratorios Conda S.A..
What is the Primary UDI-DI identifier for DESOXYCHOLATE AGAR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435295164694.
What classification code is assigned to this device?
This device is registered under product classification code W0104010101.
Similar Classification Devices (W0104010101)
Other Devices by Laboratorios Conda S.A.
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