LYSED GC SELECTIVE AGAR / SABOURAUD DEXTROSE AGAR WITH CHLORAMPHENICOL (UDI 05032384436514)
Manufactured by Oxoid Ltd
Device Regulatory Overview
The LYSED GC SELECTIVE AGAR / SABOURAUD DEXTROSE AGAR WITH CHLORAMPHENICOL (Model/Catalog Number: PB1241E) is a medical device manufactured by Oxoid Ltd. This product is indexed under FDA Product Code / Category Classification W0104010407 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PB1241E
- Product Code / EMDN
- W0104010407
- Device Name
- LYSED GC SELECTIVE AGAR / SABOURAUD DEXTROSE AGAR WITH CHLORAMPHENICOL
- Database Sync Date
- 2026-08-09 16:47:03
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 LYSED GC SELECTIVE AGAR / SABOURAUD DEXTROSE AGAR WITH CHLORAMPHENICOL?
The registered manufacturer of record for LYSED GC SELECTIVE AGAR / SABOURAUD DEXTROSE AGAR WITH CHLORAMPHENICOL is Oxoid Ltd.
What is the Primary UDI-DI identifier for LYSED GC SELECTIVE AGAR / SABOURAUD DEXTROSE AGAR WITH CHLORAMPHENICOL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05032384436514.
What classification code is assigned to this device?
This device is registered under product classification code W0104010407.
Similar Classification Devices (W0104010407)
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