ANAEROBE CDC – ANAEROBE CNA – BACTEROIDES BILE ESCULINE AGAR (BBE) (UDI 05212037701538)
Manufactured by G. PAPANIKOLAOU & CO. LP - Bioprepare
Device Regulatory Overview
The ANAEROBE CDC – ANAEROBE CNA – BACTEROIDES BILE ESCULINE AGAR (BBE) (Model/Catalog Number: 030151) 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
- 030151
- Product Code / EMDN
- W0104010499
- Device Name
- ANAEROBE CDC – ANAEROBE CNA – BACTEROIDES BILE ESCULINE AGAR (BBE)
- Database Sync Date
- 2026-08-09 16:29:11
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 ANAEROBE CDC – ANAEROBE CNA – BACTEROIDES BILE ESCULINE AGAR (BBE)?
The registered manufacturer of record for ANAEROBE CDC – ANAEROBE CNA – BACTEROIDES BILE ESCULINE AGAR (BBE) is G. PAPANIKOLAOU & CO. LP - Bioprepare.
What is the Primary UDI-DI identifier for ANAEROBE CDC – ANAEROBE CNA – BACTEROIDES BILE ESCULINE AGAR (BBE)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05212037701538.
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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