eudamed_udi
Primary ID: 05032384091911
SALMONELLA CHROMOGENIC MEDIUM (UDI 05032384091911)
Manufactured by Oxoid Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SALMONELLA CHROMOGENIC MEDIUM - Primary ID 05032384091911
Device Regulatory Overview
The SALMONELLA CHROMOGENIC MEDIUM (Model/Catalog Number: PO0958A) is a medical device manufactured by Oxoid Ltd. This product is indexed under FDA Product Code / Category Classification W0104010402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PO0958A
- Product Code / EMDN
- W0104010402
- Device Name
- SALMONELLA CHROMOGENIC AGAR
- Database Sync Date
- 2026-08-09 16:29:47
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 SALMONELLA CHROMOGENIC MEDIUM?
The registered manufacturer of record for SALMONELLA CHROMOGENIC MEDIUM is Oxoid Ltd.
What is the Primary UDI-DI identifier for SALMONELLA CHROMOGENIC MEDIUM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05032384091911.
What classification code is assigned to this device?
This device is registered under product classification code W0104010402.
Similar Classification Devices (W0104010402)
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