eudamed_udi
Primary ID: 08435295160399
BLOOD AGAR BASE (UDI 08435295160399)
Manufactured by Laboratorios Conda S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BLOOD AGAR BASE - Primary ID 08435295160399
Device Regulatory Overview
The BLOOD AGAR BASE (Model/Catalog Number: 1108) 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
- 1108
- Product Code / EMDN
- W0104010101
- Device Name
- BLOOD AGAR BASE
- Database Sync Date
- 2026-08-09 16:30:20
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 BLOOD AGAR BASE?
The registered manufacturer of record for BLOOD AGAR BASE is Laboratorios Conda S.A..
What is the Primary UDI-DI identifier for BLOOD AGAR BASE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435295160399.
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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