YERSINIA SELECTIVE AGAR (UDI 05212037700463)
Manufactured by G. PAPANIKOLAOU & CO. LP - Bioprepare
Device Regulatory Overview
The YERSINIA SELECTIVE AGAR (Model/Catalog Number: 010132) is a medical device manufactured by G. PAPANIKOLAOU & CO. LP - Bioprepare. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 010132
- Product Code / EMDN
- W0104010405
- Device Name
- YERSINIA SELECTIVE AGAR
- Database Sync Date
- 2026-08-09 18:58:34
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 YERSINIA SELECTIVE AGAR?
The registered manufacturer of record for YERSINIA SELECTIVE AGAR is G. PAPANIKOLAOU & CO. LP - Bioprepare.
What is the Primary UDI-DI identifier for YERSINIA SELECTIVE AGAR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05212037700463.
What classification code is assigned to this device?
This device is registered under product classification code W0104010405.
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