BLOOD AGAR – MAC CONKEY AGAR – SABOURAUD DEXT. AGAR (UDI 05212037700982)
Manufactured by G. PAPANIKOLAOU & CO. LP - Bioprepare
Device Regulatory Overview
The BLOOD AGAR – MAC CONKEY AGAR – SABOURAUD DEXT. AGAR (Model/Catalog Number: 030152) is a medical device manufactured by G. PAPANIKOLAOU & CO. LP - Bioprepare. This product is indexed under FDA Product Code / Category Classification W0104010499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 030152
- Product Code / EMDN
- W0104010499
- Device Name
- BLOOD AGAR – MAC CONKEY AGAR – SABOURAUD DEXT. AGAR
- Database Sync Date
- 2026-08-09 17:45:21
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 – MAC CONKEY AGAR – SABOURAUD DEXT. AGAR?
The registered manufacturer of record for BLOOD AGAR – MAC CONKEY AGAR – SABOURAUD DEXT. AGAR is G. PAPANIKOLAOU & CO. LP - Bioprepare.
What is the Primary UDI-DI identifier for BLOOD AGAR – MAC CONKEY AGAR – SABOURAUD DEXT. AGAR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05212037700982.
What classification code is assigned to this device?
This device is registered under product classification code W0104010499.
Similar Classification Devices (W0104010499)
Other Devices by G. PAPANIKOLAOU & CO. LP - Bioprepare
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