AGAR SELETIV YERSINIA (UDI 05940540374825)
Manufactured by Sanimed International Impex S.A.
Device Regulatory Overview
The AGAR SELETIV YERSINIA (Model/Catalog Number: 20549) is a medical device manufactured by Sanimed International Impex S.A.. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20549
- Product Code / EMDN
- W0104010405
- Device Name
- AGAR SELETIV YERSINIA (YERSINIA SELECTIV AGAR)
- 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 AGAR SELETIV YERSINIA?
The registered manufacturer of record for AGAR SELETIV YERSINIA is Sanimed International Impex S.A..
What is the Primary UDI-DI identifier for AGAR SELETIV YERSINIA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05940540374825.
What classification code is assigned to this device?
This device is registered under product classification code W0104010405.
Similar Classification Devices (W0104010405)
Other Devices by Sanimed International Impex S.A.
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